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Last modified
8/11/2009 11:28:21 AM
Creation date
8/10/2009 5:17:40 PM
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UCREFRP
UCREFRP Catalog Number
9722
Author
Hilderbrand, R.H., A.C. Watts and A.M. Randle.
Title
The myths of restoration ecology.
USFW Year
2005.
USFW - Doc Type
Ecology and Society
Copyright Material
YES
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<br />tI. <br /> <br />Wilson 1996, Mitsch et al. 1998) is embraced after <br />the hydrologic conditions are restored. Restoration <br />sites do become revegetated, but may be of different <br />species composition and degree of cover (Seabloom <br />and van der Valk 2003), owing to dispersal <br />limitations of many wetland species (Galatowitsch <br />and van der Valk 1996). Thus, the effectiveness of <br />self-design depends on the restoration goals, but <br />adopting a concept of self-design does implicitly <br />recognize and embrace the existence of multiple end <br />points. <br /> <br />An effective restoration of the physical variables <br />will create the template for biotic recovery, but <br />physical structure does not always beget biotic <br />structure, and biotic structure does not necessarily <br />result in similar ecosystem functions across sites. <br />The concept of self-organization, or self-design, is <br />an intuitively appealing approach and is very <br />attractive to resource managers who have limited <br />time and budgets. A self-assembling ecosystem <br />would substantially cut down on the amount of <br />effort required to restore ecosystems, and we feel <br />this is why the Field of Dreams is commonly <br />employed. However, its effectiveness in restoring <br />structure and function is still debatable (Simenstad <br />and Thom 1996, Zedler and Callaway 1999, <br />National Research Council 2001), and restored <br />areas may be quite different from undisturbed sites <br />(Seabloom and van der Valk 2003). In defense of <br />self-assembly, composition of restored sites is <br />expected to approach reference sites given sufficient <br />time (Mitsch 1997). Effective restoration using this <br />approach must overcome issues of recolonization <br />and dispersal, stochasticity in community assembly, <br />and assembly of energy transfer pathways. One <br />commonly used strategy to circumvent these <br />limitations is to jumpstart the process by adding <br />organisms, but our understanding of accelerating <br />ecosystem development is incomplete and may lead <br />to the myth of Fast-Forwarding. <br /> <br />THE MYTH OF FAST-FORWARDING <br /> <br />The myth of Fast-Forwarding is based on the idea <br />that one can accelerate ecosystem development by <br />controlling pathways, such as dispersal, colonization, <br />and community assembly, to reduce the time <br />required to create a functional or desired ecosystem. <br />This idea stems from the initial floristics model of <br />succession (Egler 1954) in which the process of <br />ecosystem development is accelerated by <br />controlling initial species composition and <br /> <br />Ecology and Society 10(1): 19 <br />htto:/ /www.ecolol!.Vandsocietv.orl!lvoII0/issl/artI9/ <br /> <br />succession to achieve the desired end point (van der <br />Valk 1998). The major assumption is that we can <br />reliably recreate key processes and links between <br />the biota and physical environment. A driving force <br />behind this approach is the need to demonstrate <br />rapid recovery of disturbed lands in order, for <br />example, to have insurance or mitigation <br />performance bonds returned quickly. <br /> <br />Many types of restoration projects justifiably use a <br />fast-forwarding approach to jumpstart the recovery <br />process by using species desired in the ecosystem. <br />As most restorations include plantings to get the ball <br />rolling and stabilize the terrain, it is logical to try to <br />advance the successional process, and this is why <br />the practice is so common. However, relying on the <br />premise that fast-forwarding will produce the <br />desired ecosystem trajectory and speed the recovery <br />process may result in disappointment. Little <br />evidence exists for achieving desired trajectories or <br />functions within the shortened time spans promised <br />by fast-forwarding (Simenstad and Thom 1996, <br />Zedler and Callaway 1999, Campbell et al. 2002, <br />Wilkins et al. 2003). As with other myths, there is <br />some element of truth, and successes using fast- <br />forwarding have occurred (e.g., Clewell 1999). <br />Successful projects typically require multiple <br />plantings and a considerable amount of attention to <br />ensure survival of plantings in systems that may be <br />"premature" for the species' arrival. Even when <br />successful, certain ecological processes, such as the <br />development of tree hollows for cavity-nesting <br />animals, soil development, mycorrhyzal associations, <br />and hydrologic regimes, present more difficult <br />challenges and may take years or decades. Mitsch <br />and Wilson (1996), for example, point out that the <br />5-year span in which "'quick-fIX' wetlands" are <br />expected to become sufficient replacements for lost <br />or damaged areas is improbably short, and that 15- <br />20 years is a much more realistic expectation. Long- <br />term monitoring ( 5-15 years) of restoration projects <br />is indicating that a more likely time horizon is <br />several decades for a restoration to resemble a pre- <br />disturbance target (Zedler and Callaway 1999, <br />Wilkins et al. 2003). Many ecological restoration <br />projects--even ecological restoration itself-aim <br />for rapid progress from a damaged state toward <br />some more-or-less specific target. There is nothing <br />inherently wrong with such a goal, however, we <br />should not be so intent on attaining a specific point <br />that the system's potential future state (i.e., after <br />restoration efforts cease and natural processes take <br />over) is ignored. <br />
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