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1 Samuel M. Scheiner and Michael R. Willig, eds. 1. A General ...

1 Samuel M. Scheiner and Michael R. Willig, eds. 1. A General ...

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groups, colonies, or symbiotic systems, or to coevolved multispecies systems. From this<br />

perspective, the model is not general at all. It is just one in a collection of complementary, <strong>and</strong><br />

sometimes interacting or overlapping, models. By having a narrow scope, the model can be<br />

reasonably realistic if parameters are estimated for a limited natural universe. Still, models of<br />

populations, or interactions among populations in different contexts, are a major stronghold of<br />

theory in ecology.<br />

By contrast, ecosystem models are often developed for specific natural systems (Fitz et<br />

al. 1996). Such models rely on general physical principles to account for the energy <strong>and</strong> material<br />

budgets <strong>and</strong> on biological relationships to provide system specific <strong>and</strong> local contents. They can<br />

be quite realistic, at least this is the intention of the investigators, but attempts to make them<br />

general would require stripping biological contents <strong>and</strong> so removing these models from the<br />

domain of ecology. In any case, I believe that ecology has benefited from developing <strong>and</strong><br />

accumulating ecosystem models in several ways such as building bridges to cybernetics <strong>and</strong><br />

engineering, providing management tools (e.g., adaptive management – Holling 1978), <strong>and</strong><br />

explicitly incorporating the abiotic environment into the dynamics of ecological systems.<br />

Still another category of models appears to be driven by the need for precision. In an<br />

attempt to explain species rank-abundance distributions ecologists developed a number of<br />

statistical models. They are judged by the precision with which they describe actual collections<br />

of data. In the absence of a good theory about underlying mechanisms, these models cannot be<br />

seen as general. In fact, these models seem to work well in particular situations only, for<br />

example, large data sets from undisturbed habitats generally follow a log-normal model of<br />

abundance distribution. Different may models apply to disturbed habitats or small data sets. As<br />

these models do not make good explicit links to underlying processes, they can hardly be seen as<br />

realistic, even when they provide a precise fit to the data.<br />

It is surprising, <strong>and</strong> it holds some promise, that some of the early, potentially important,<br />

concepts have not advanced theoretically for over 100 years. Forbes’ microcosm embodied the<br />

idea of wholeness <strong>and</strong> relative autonomy. He articulated, early on, a central notion that the<br />

ecological world exists in the form of aggregates of interdependent parts. In his view, this<br />

aggregation would be responsible for the emergence of partially bounded systems whose<br />

components with a appreciable ability to adjust internally to each other. It is rather surprising<br />

that this idea, while often invoked in the context of conservation, has not developed theoretically<br />

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