Chaos!The Verhulst equation is the name used for the equation we studied in the last section when it is applied to modeling ecological populations. We can study this dynamic system more generally, and then we refer to it as the Logistic Function. We will explore the sensitivity of this equation to different starting values of the population P, and of the fertility factor C. The Logistic Function
Pn+1 = Pn + CPn(1-Pn)
The applet below lets us explore the behavior of the Logistic Function. You can click and drag the parabola in the left
panel up and down which serves to change the value of C,
the fertility. You can also <Shift>-click and drag left and right to adjust the starting value, P0. The right panel shows the value of the equation (say, population) on the Y-axis and the X-axis represents time. Drag the blue parabola in the left panel up and down and see what happens. By doing this, you can change the value of C from 0 to 4. Make sure to keep P0 = 0.5 for now.
Watch the behavior of the population in the right panel as a function of time.
At first, say at C=2.6 the population oscillates briefly but soon converges on a single value. This is seen in the graphical iteration on the left
as the red line spiraling in to the single solution where the parabola crosses the diagonal line.
By the time you raise the value of C to 3.2, the population in the right panel is stably oscillating between two values. This is simple periodic behavior, with a
period of 2. In the left panel this corresponds to the graphical iteration in the left panel following a simple path between two solutions, the points
where the red line touches the parabola. Keeping dragging up the parabola. Between 3.5 and 4.0 the behavior of the Logistic Function is extremely complex. This shows up in the left panel as lines intersecting the parabola
in a large number of points, and in the right panel as generally aperiodic (i.e. not periodic) behavior. This means that the population fluctuates erratically, rather than in a simple periodic manner.
Although if you look carefully, you can find a number of places where the equation does behave periodically, with various higher-order periods. For instance at C = 3.8375, the
equation briefly returns to a stable period 2 behavior.
At some ranges, the Logistic Function is exquisitely sensitive to small changes in the value of C. It can also be very sensitive to changes in the starting value of the population. Set the value of C to 3.6625. Hold down <Shift> and drag sideways in the left panel to change the value of P0. Observe that the behavior of the equation is very sensitive to changes in the starting value of the population. Change the number of iterations in the input field at the top right to 100 to see a longer data set. Be careful drawing conclusions about the behavior of the equation! Something that might look periodic, may eventually break down into disorderly, irregular behavior. Or,
something may start off erratically, but after many iterations it may converge to a stable periodic orbit. What lessons can we draw from this behavior about population ecology in the real world? First of all, we must be careful in drawing conclusions, because this equation
is a gross over-simplification, dealing with a single species and only two variables. But one lesson is that a system can abruptly change from alternating periodically to
behaving unpredictably and erratically. And then switch back abruptly to regular behavior. Chaos theory teaches us to approach dynamic systems cautiously. For while there
is often great stability built into networks of interacting systems, it is also true that small changes to a system can spiral out of control, and cause all sorts
of unpredictable outcomes.
There are many times when we inadvertently manipulate these parameters in the real world. For instance, when a road is built through a wilderness area, it may only reduce
the total area of the wilderness by a miniscule amount. However, roads often functionally subdivide an ecosystem into two disconnected populations of animals.
This may have drastic impacts on the population dynamics, because the starting value of each of the two sub-populations is much lower than that of the intact population. Ecologically, two
adjacent ecosystems with a barrier between them may behave completely differently from an intact ecosystem.
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