(Attractiveness vs. Efficiency)
8 Observations
For the sake of more controlled experiments and predictable results, the choice of
what is attractive was taken out of the hands (or genes, as it were) of the swimbots.
The 'favorite color' gene was removed, and the criteria for attractiveness were set
up as the objectively-defined features (as described earlier). When attractiveness was
set to equal Massiveness, the simulation produced thick-bodied swimbots which moved
slowly, as expected. When it was set to equal Movement, large motions became the norm,
and consequent swimming strategies became aggressive and bold. Openness resulted in
bodies which were spread-out more, as illustrated in Figure 8, where each image
represents 3 time steps. The population represented in this illustration exhibited a
curious behavior: the stroke recovery (at the beginning and end of this sequence)
appears more exaggerated than what would normally be expected.
It is as if the
swimbots had overshot the motion, and opened-up inside-out. This behavior might have
given some swimbots a slight advantage in being chosen. A pursuing swimbot sizing up
mates can take a snapshot of a potential mate at any stage of its swim cycle to
measure its attractiveness. Therefore, exhibiting open features through the majority
of the swim cycle creates an advantage.
Attraction to Length resulted in
unique behavior: bodies became extremely long, with few branches in their topology.
The 'parent' genes (for part connectivity) had adapted to become more sequential.
Figure 9 illustrates a group of swimbots from a population which evolved with this
criteria. These swimbots exhibit very rigid postures, using a small paddle-like part
at the end to propel forward. Over evolutionary time these paddling behaviors were
replaced by graceful undulating motions in straight bodies.
Figure 9. A group of long swimbots
The Virtues of Vegetating
Setting attraction to be the inverse of
these features revealed interesting results. For instance, in a simulation run in
which attractiveness was set to equal lack of movement, the simulation produced a
population of swimmers with sparse anatomy, and with very little motion. This
simulation resulted in lower average energy efficiency than most other simulation
runs (the time series graph which is not illustrated here reveals a relatively low,
uneventful energy efficiency trend). A few qualitative observations were made from
this simulation.
Since the simulation had produced swimbots who moved slowly,
the fluid field exhibited a great patchwork quilt of phenotypes
(indicated by coloration), since genotypes mixed at such a slow rate.
Mating remained predominantly local. All swimbots however were very simple in
anatomy, possessing only two parts, as shown in Figure 10.
Another observation was made: although swimming was slow, swimbot population rose
dramatically. The explanation may be that since swimbots expended little energy,
they were able to live long lives: a lower death rate. This large population then
offered those few swimbots who were slightly mobile a wealth of potential mates
within close proximity. Locomotion required for reproduction was not demanding of
energy or time.
Figure 10. A family of slow swimbots from a population attracted to lack of movement
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