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Defining Restoration Goals <br />*at the ecosystem -level framework encourages res- <br />torationists to both pay attention to landscape -level dy- <br />namics and to attempt to integrate an understanding of <br />these large -scale processes with the small-scale processes <br />of soil ecology and species biology. He also points out <br />that the "management" part of the phrase encourages <br />thinking about the widest possible range of interventions <br />that affect both large- and small-scale processes. <br />The use of ecosystem -level goals for restoration and <br />conservation has been strongly criticized, in large part be- <br />cause key concepts and terms are poorly defined (Gold- <br />stein 1999) (Table 1). For example, the idea of ecosystem <br />management suffers from vagueness in the definition of <br />ecosystem, as well as in the definitions of other terms used <br />to define the goals of ecosystem management (i.e., ecosys- <br />tem integrity or ecological health) (Wilcove & Blair 1995). <br />Allen (1996) has pointed out, however, that many of the <br />concepts used in species -based conservation and restora- <br />tion are similarly vague. "Minimum viable population <br />size" can be given a mathematical definition, but is hard to <br />apply to real -life situations. Levels of anthropogenic dis- <br />turbance and pollution that affect the health of popula- <br />tions are vigorously debated (for example, the controver- <br />sies over organochlorine pollutants in the Great Lakes and <br />iiieffects on organisms [Carpenter 1995; and related ar- <br />]). The goal of conservation biology that "compo- <br />nents of the ecosystem should [not] be perturbed beyond <br />natural boundaries of variation" (Mangel et al. 1996, p. <br />338) leaves open the definitions of what are the "compo- <br />nents of the ecosystem" (never mind the definition of eco- <br />system) as well as what are the natural boundaries of vari- <br />ation. Many other examples could be cited. Lack of <br />precision in the definition of ecological terms has been a <br />controversial issue for decades in ecology as a science, but <br />has not prevented its effective application in both conser- <br />vation and restoration. Thus, although criticisms of the <br />vagueness of terms used to develop ecosystem based <br />goals may be legitimate (Goldstein 1999), the same criti- <br />cisms apply to other foci for restoration. To deny the im- <br />portance of ecosystem -level processes because of prob- <br />lems of definition ignores both the importance of these <br />processes and the long history of using poorly defined <br />terms to good purpose in many specific cases of restora- <br />tion and conservation. <br />However, even if we accept the fuzziness of the gen- <br />eral concepts invoked in ecosystem management and <br />restoration, there are additional problems of definition <br />that hamper the use of ecosystem functions as a basis for <br />restoration goals (Table 1). The fundamental premise of <br />this approach is the recognition of ecosystem processes, <br />11111ctions, that create and drive the system, and that <br />D1Oth a result of structure (e.g., species composition) <br />and a causative factor in creating structure. However, the <br />concept of ecosystem function is equally vague. Every <br />discussion of this idea lists a somewhat different set of <br />items. Table 2 lists an amalgam of items culled from a va- <br />riety of sources; it is as idiosyncratic and individualistic <br />as (and has no greater validity than) any other list. The <br />point is that the processes that make up ecosystem func- <br />tion are as variable as the definition of ecosystem itself. <br />Just within this list, there is tremendous heterogeneity. <br />Some processes, such as nutrient cycling or .energy flow <br />integrate the activities of numerous organisms (e.g., the <br />extraordinary, if poorly recognized, diversity of soil or- <br />ganisms; Wall & Moore 1999). Others, such as succession <br />or mutualisms, reflect the biology of particular species <br />and are population -level phenomena, rather than ecosys- <br />tem processes as usually defined. Some processes (e.g., <br />diversity) reflect purely biological phenomena, whereas <br />others reflect purely physical phenomena (disturbance <br />regimes caused by storms) and still others reflect com- <br />plex mixtures of biological and physical forces (soil for- <br />mation and water quality). The items in Table 2 are also <br />heterogeneous in terms of the scales of space and time <br />over which they apply and over which they are mea= <br />sured. Some items (e.g., succession and mutualisms) are <br />variously included or excluded from lists of ecosystem <br />functions, depending on the viewpoint of the list - maker. <br />Measurable components of each of the processes <br />listed in Table 2 have the same problems of heterogene- <br />ity, although they are more readily definable. Table 3 <br />lists, as examples, the quantifiable components of three <br />of the most commonly cited ecosystem functions. <br />Again, the measurable components of each process are <br />heterogeneous with respect to the time and spatial <br />scales of the phenomena they index, and heterogeneous <br />Table 2. Processes included under the rubric "ecosystem <br />functions." <br />Category <br />Process <br />Material flow <br />Physical elements <br />Biological structure <br />Energy flow <br />Nutrient cycling <br />Nutrient retention /loss <br />Carbon storage <br />Productivity <br />Water flow <br />Water turnover rates, flow rates <br />(aquatic) <br />Transfers to /from other ecosystems <br />Disturbance regimes (fire, disease, <br />storms) <br />Water quality <br />Landscape structure <br />Soil formation <br />Trophic structure <br />Predation /herbivory rates <br />Succession <br />Resilience /resistance <br />Diversity <br />Mutualisms <br />Passive vs. active dispersal <br />MARCH 2000 Restoration Ecology <br />5 <br />