The notion that we might think of human populations as represented
by the reaction-diffusion equation was, rather surprisingly, first
hypothesized by Harold Hotelling (1921), the great
statistician/economist responsible for so many imaginative and important
papers over a career that began in the mid-1920s. What is not generally
known is that Hotelling actually began his education not as an economist
or statistician, but as a journalism student, receiving a
bachelor's degree from the University of Washington in Seattle in
1919. He then decided to undertake further study for a master's
degree, but in mathematics rather than journalism. His M.S. Thesis
submitted to the Department of Mathematics at the University of
Washington in 1921 is entitled "A Mathematical Theory of
Migration." The existence of this thesis is little known, but it
foreshadows Hotelling's brilliant career and elegant modeling
ability. Hotelling's thesis basically proposed that we think of the
westward movement in the United States as a reaction-diffusion process.
As he wrote:
(if we hypothesize) that the percentage rate of
natural increase at any place is proportional
to the difference between the density of population
and a fixed saturation point, ... we have
[partial derivative][pi]/[partial derivative]t =
K[[nabla].sup.2][pi] + [alpha][pi]([sigma] - [pi]) (39)
This equation is not linear, and is difficult to handle. But as we
have seen, we may be dealing with new and sparsely settled countries
assuming a Malthusian principle that population increases in a geometric
ratio; while for countries near the saturation point it is not
unreasonable to assume that the number of births per unit of area is
proportional to the difference between the density of population and the
saturation point. For the first case, we combine equation (20) with (1);
for the second we take (20) and (3). These give respectively
[partial derivative][pi]/[partial derivative]t = K[[nabla].sup.2]
[pi] + r[pi] (40)
and
[partial derivative][pi]/[partial derivative]t = K[[nabla].sup.2]
[pi] + b([sigma] - [pi]) (41)
The elegance of Hotelling's approach is admirable. He first
proposes the general reaction-diffusion equation to model the westward
movement (his notation for diffusion used the diffusion coefficient K,
the more general gradient symbol [[nabla].sup.2] for the second partial
derivative and the symbol [pi] for the population at any point). His
justification for the simple Fick's Law type of diffusion process
is, however, not the assumption that movement is random. Instead, he
proposes that settlers move from high- to low-density areas for economic
reasons (in search of low-cost land, for example). Then they will act as
if they are diffusing randomly via Fick's Law, even though there is
behavioral purpose driving movement. As he notes, the reaction-diffusion
equation "is difficult to handle" (an understatement, since it
was not really understood until sixteen years later) and hence he
proposes solving two simpler problems, the solutions of which can
actually be derived explicitly, and which qualitatively bracket the more
general problem.
The remainder of Hotelling's thesis is empirical. He procures
the U.S. census records for the 1790-1900 period and uses the data to
compute the implied diffusion coefficients of the actual westward
movement "wave front," thus calibrating the model to complete
his analysis. Aside from the cleverness and elegance of thought that the
thesis reveals in the young Hotelling, it also is the first depiction of
a spatial-dynamic process driven by economic behavior depicted by a
diffusion mechanism.
To summarize, the fundamental drivers of spatial-dynamic processes
are diffusion or dispersal processes. These can be modeled with partial
differential equation descriptions. As shown above, there is a rich
variety of diffusion models available to fit circumstances ranging from
simple random movement, to advection to joint diffusion/population
growth. A few of these models can be solved analytically, but most
cannot. This presents analysts of spatial-dynamic problems with
challenges. There are essentially two ways to build understanding of
these kinds of complex situations. One way is to construct numerical
models of complex systems and attempt to synthesize some common
understanding from the analysis of a range of cases. The other way is to
start with very simple models, extracting what can be learned before
adding detail. This is the method we illustrate next, using a familiar
current policy problem.
An Example: Bio-Invasions
To illustrate how we might model spatial-dynamic processes in order
to gain understanding about policy options, I will now turn to an
example, namely the example of bioinvasions. Bio-invasions are familiar
to everyone, and there are numerous cases that come to mind, including
kudzu, the gypsy moth, yellow starthistle, and zebra mussels.
Bio-invasions are successful colonizations of alien species that have
been either accidentally or purposefully introduced into ecosystems.
They may generate damages (or benefits) as they spread, and costs of
control depend upon when, how intensively, and where control activities
are undertaken.
Bio-invasions are becoming increasingly prominent in the public
eye, and the topic has also received considerable research attention,
first by ecologists but more recently by economists. For the most part,
however, economists have ignored the spatial-dynamic aspects of
bio-invasions, often treating them as little more than a pest-control
problem. This seems to miss the most interesting aspect of
bio-invasions, namely their spatial-dynamic character. While simple
characterizations that address questions such as whether to spray or
not, or whether to quarantine or not are illuminating, the more
important questions seem to be where to spray, when, and at what
intensity in a landscape setting. (3) This requires a modeling apparatus
that captures essential features of spatial-dynamic problems.
The economic issues that bio-invasions raise are several. How does
an uncontrolled bioinvasion unfold? What governs its rate of spread, and
how fast is that spread if no actions are taken? What are the
consequences to humans of the invasion? What kinds of actions are
available to control a bio-invasion? At what points over time and space
are instruments available to manage the bio-invasion? What is the
optimal way to use controls; when, where, and how intensively should
they be implemented? How is the optimal control affected by bio-economic
parameters? How do basic cost/benefit parameters affect the best choice?
How about the discount rate and time horizon? Does the optimal control
vary with the initial size of the invasion? If an invasion is uncertain,
what kinds of monitoring and detection efforts should be implemented?
Answering these kinds of questions requires some kind of modeling
effort. The modeling should first describe the biophysical diffusion
mechanisms that drive the bio-invasion. Diffusion may occur in a smooth
and homogeneous pattern over space, driven by short-term dispersal
processes such as simple local movement. For example, the classic case
in biology textbooks of muskrat spread in Europe reveals a stark radial
pattern with a predictable velocity of the "wave front" over
several decades (Murray 2002), much like predicted by the Fisher
reaction-diffusion equation. Alternatively, dispersal may involve
long-distance mechanisms driven by wind and currents, or by movement of
hosts including humans, animals, and birds (Hastings et al. 2005). A
model of a bio-invasion should also incorporate some assumptions about
boundaries and processes that occur at boundaries, as well as the
geometry of the relevant space. Finally, a model of bio-invasions needs
to reflect humans and define the links between humans and biophysical
environment. Are humans simply passive participants, or do they
influence the spatial-dynamic patterns by their actions? How are humans
impacted by the bio-invasion? Once these critical components, the
biophysical systems with its dispersal mechanisms and spatial character
and the human linkages, are specified, the system can be simulated and
optimized to generate some predictions of the consequences of various
policy options. Further refinements can then be added if necessary and
policy conclusions expanded.
[FIGURE 3 OMITTED]
A Simple Bio-invasion Model
Consider the simplest possible model of a bio-invasion that
incorporates the above elements, albeit in the most abstract fashion.
Suppose that we consider the spatial geometry of our model system to be
a corridor of fixed width, with the origin at the left-hand side, and an
unbounded right-hand side. As in figure 3, we assume that there is an
initial invasion that is discovered after having covered an area of
amount [X.sub.0]. The invasion is assumed to spread along the length of
the corridor with a velocity of v. (4) The area infested at any date t
will be X(t) = [X.sub.0] + vt. Assume that damages are proportional to
the total area infested in each period, where the marginal damage per
unit space is d. I have in mind something like star thistle, a weed that
spreads through pasture land and that grazing animals will not eat.
Assume that control costs are incurred each period in a manner that
influences the velocity of the wave front of the invasion (Sharov and
Liebhold 1998). If [bar.v] is the natural velocity of the uncontrolled
bioinvasion, let control costs be quadratic in the velocity reduction
associated with control activities, or:
TC(v) = a([bar.v] - v) + (1/2)b[([bar.v] - v).sup.2]. (6)
[FIGURE 4 OMITTED]
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