Modeling has become an important tool in ecology. There are many
reasons why an ecological system or process cannot be directly manipulated in a
field test and therefore why a mathematical approach becomes necessary. For
example, realistic funding restrictions prevent ecologists to carry on
large-scaled and long-term trimming experiments for testing community responses
to an environmental disturbance. Models can help explore ideas in regards to
one’s thinking, define questions more precisely, assist in testing hypotheses,
and identify data needs.
More and more ecology students consider modeling as an essential
component of their education. However, some students may be mislead to think
that ecological models (particularly those dealing with ecosystems and
communities) are extremely complex and detailed, and filled with intractable
mathematical equations. In reality, an ecological model can be as simple as a
visual representation in which two species are connected by an arrow to
represent some relationship, such as predator and prey. A complex system can
thus be represented by and analyzed from a relatively simple visual
representation. This modeling approach is called qualitative modeling, or loop
analysis. It is more practical than quantitative modeling, because qualitative
models require fewer resources and less modeling experience. Mostly
importantly, qualitative models are critical in defining research questions.
As used in mathematical ecology, qualitative modeling is simply a
rigorous analytical approach of complexity. It applies well established
mathematical concepts, some dating back over a century. It emerged in its
present conception in the 1960’s following the efforts of economists, whose
work strongly influenced the theory of community ecology in the following
decades, led mostly by Robert May and Richard Levins. The availability of
symbolic processors for PCs and novel mathematical advances have led to a renew
interest in the approach.
Qualitative models are typically drawn as diagrams, called signed
digraphs, with circles and lines that represent the ecological variables and
flows of materials, energy, or causation between two variables, respectively.
If there is a direct positive effect of one variable upon another, the line
will be ended in a pointed arrow. A line with a solid circle at the end of it
represents a negative interaction. An absence of line means no direct
interaction between two variables. Thus, the interactions between populations
of different species in a community can be classified according to combinations
of the three symbols {–,0,+}. In general, there are 5 types of interactions:
predator-prey (+/-), interference (-/0), mutualism (+/+), commensalism (0/+),
and amensalism (0/-). Since it is difficult, or often impossible, to fully
understand the quantitative relationship between two variables, a qualitative
specification of an ecological system is often the best that ecologists can do.
Simply knowing the sign of their interactions can provide important insights to
the dynamic behavior of complex systems. Thus one can “draw” an ecological
community system just based upon his knowledge of species interaction. The
signed digraph is then converted to a community matrix with only three numbers
{-1,0,1}. Several matrix algebra functions are used to test the system and
predict the behavior of system response to a disturbance. Because of its
simplicity, qualitative modeling is now becoming accepted as a standard
approach in biology.
The two analyses that have become standard are of stability and
of predictability. In evaluating stability, a system is assessed for conditions
under which stability is possible. Novel criteria allow provide greater insight
and subtlety in evaluations of stability (Dambacher, Luh, Li and Rossignol
2003). The response of the density of variables of the system to a sustained
perturbation can then be assessed, or ‘predicted’ based on a probabilistic
scale (Dambacher, Li and Rossignol 2002). A novel algorithm now provides
predictions of changes in life expectancy as well (Dambacher, Levins and
Rossignol 2004).