SPECIAL SECTION BIOTROPICA 42(1): 10–20 2010 10.1111/j.1744-7429.2009.00567.x The Importance of Defining ‘Forest’: Tropical Forest Degradation, Deforestation, Long-term Phase Shifts, and Further Transitions Francis E. Putz1 Department of Biology, University of Florida, Gainesville, FL 32611-8526, U.S.A. and Kent H. Redford Wildlife Conservation Society, 185th and Southern Boulevard, Bronx, NY 10460, U.S.A. ABSTRACT While research continues on the causes, consequences, and rates of deforestation and forest degradation in the tropics, there is little agreement about what exactly is being lost, what we want back, and to whom the ‘we’ refers. Particularly unsettling is that many analyses and well-intended actions are implemented in fogs of ambiguity surrounding definitions of the term ‘forest’—a problem that is not solely semantic; with development of markets for biomass carbon, vegetation classification exercises take on new relevance. For example, according to the basic implementation guidelines of the Kyoto Protocol, closed canopy natural forest could be replaced by monoclonal plantations of genetically engineered exotic tree species and no deforestation would have occurred. Following these same guidelines, carbon credits for afforestation could be available for planting trees in species-rich savannas; these new plantations would count towards a country moving towards the ‘forest transition,’ the point at which there is no net ‘forest’ loss. Such obvious conflicts between biodiversity conservation and carbon sequestration might be avoided if ‘forest’ was clearly defined and if other vegetation types and other ecosystem values were explicitly recognized. While acknowledging that no one approach to vegetation classification is likely to satisfy all users at all scales, we present an approach that recognizes the importance of species composition, reflects the utility of land-cover characteristics that are identifiable via remote sensing, and acknowledges that many sorts of forest degradation do not reduce carbon stocks (e.g., defaunation) or canopy cover (e.g., over-harvesting of understory nontimber forest products). Key words: biodiversity; carbon sequestration; climate change; land-use change; plantation; REDD; savanna; scrub. DESPITE LACK OF CONSENSUS OVER WHAT IS AT STAKE, multitudes of efforts are underway to protect forests, to manage them sustainably where outright protection is not a viable or desirable option, to restore them where they are degraded, to re-create them where they have been lost, and to create them anew in areas that were not historically forested. These efforts are motivated by a variety of concerns including the desire to maintain or restore ecosystem functions (e.g., biogeochemical cycles), to protect biological diversity, to make money, to improve the welfare of rural people, to wrest control of land from rural people, and to preserve opportunities for research and recreation. Unfortunately, discussions about forests and their fates are plagued by fundamental differences in what different people mean when they invoke the term ‘forest’ (Lund 2002, Perz 2007). We argue that instead of being simply semantic, these differences have potentially grave conservation, development, climate, and livelihood consequences. In particular, the commodification of biomass carbon makes clarification of vegetation and land cover classification terms critical lest biodiversity, human welfare, and other ecosystem services be jeopardized. We stress that if people are careful to specify the ecosystem states they have in mind, then communication and conservation will both be fostered. While endeavoring to clarify what is meant by ‘forest’ and the names used for other vegetation types, we realize that no one classification system is ever going to be accepted by all relevant stakeReceived 26 August 2008; revision accepted 19 April 2009. 1 Corresponding author; e-mail: [email protected] 10 holders, nor is it likely to be appropriate for all applications (e.g., global vegetation mapping, estimating carbon stocks, monitoring biodiversity losses, and fostering sustainable management). Foisting a classification system on stakeholders who do not share our predominantly Western scientific vision and our biome biases is not our intention. Furthermore, we recognized that the boundaries between categories in any classification system are unavoidably fuzzy and sometimes overlapping. These limitations notwithstanding, we present an approach to ecosystem classification that can be adapted to local conditions, that will improve communication, and that should promote the success of conservation and development efforts. Our focus is on forests and their derivatives, which is itself worrisome insofar as whatever classification system is used, it is imperative that ecosystems other than forests be recognized. Our concern is that if tropical landscapes are falsely portrayed as either being forested or nonforested, other valuable ecosystems will be put in jeopardy. Furthermore, use of this false dichotomy could obscure substantial losses in ecological values (e.g., carbon losses from natural forest degradation; Foley et al. 2007, Tucker et al. 2008) from areas that still qualify as being forested. Finally, when a country or province is reported to have passed the ‘forest transition’ (sensu Mather 1990) from net forest loss to forest recovery, what was lost could be very different from what is being gained if unclear or overly simple definitions of ecosystem states are used (e.g., plantations are treated as forests). In this paper we discuss the historical bases for classifying an area as being forested and then examine some of the ways the term r 2009 The Author(s) Journal compilation r 2009 by The Association for Tropical Biology and Conservation SPECIAL SECTION Importance of Defining ‘Forest’ ‘forest’ has been used in social, political, and scientific discourse. We endeavor to show why people engaged in debates over the fates of forests, particularly in the tropics, should be explicit about the perceived starting conditions and desired ending conditions of the ecosystems under consideration (Farley 2007). WHAT IS ‘FOREST’? ENGLISH ETYMOLOGY AND POWER POLITICS Excavating the historical roots of the word ‘forest’ serves mostly to illustrate the contradiction between the modern use, which implies an area with a closed canopy of trees, and the word’s original meaning (e.g., Young 1979, Harrison 1992, Agnoletti & Anderson 2000, Vera 2000). Apparently the term was first used in English to indicate uncultivated land of a variety of vegetation types, including grasslands, which were claimed by royalty. In a process that continues to this day, 7th Century Frankish kings claimed rights to forestis, uncultivated hunting and swine foraging areas with no clear owner (at least from the royal perspective). This interpretation is based on forestis being derived from the Latin foris, which can mean ‘outside the settlement’ (Harrison 1992). Rackham (1998) made the case that in England, ‘forest’ traditionally meant a place with deer. When William the Conqueror of Normandy invaded in 1066, he built on this concept with his Forest Law, which proclaimed his sovereign rights to all wild animals, particularly deer. This effort at securing the rights to game and other natural resources codified the desires of Anglo Saxon rulers for dominion over hunting grounds (Perlin 1991). From such royal attempts at criminalizing traditional uses and securing dominion over uncultivated lands spring the tales of Robin Hood of Sherwood Forest (Watkins 1998), the War of the Demoiselles over forest access in 19th Century France (Sahlins 1994), the sultanization and then federalization of Javan teak ‘forests’ (Peluso 1992), and ongoing struggles over land-use rights in many developing countries in the tropics (e.g., Westoby 1989, Dawkins & Philip 1998). What is too often overlooked in discussions about forest-use rights through history is that while the basic social issue of contested access remains relevant, uses of the term ‘forest’ have continued to evolve. In much of the tropics where the rights of indigenous peoples are often in contention, ‘forest’ is often defined on cultural grounds (e.g., Brosius 1997). Given the global focus on forest conservation, there is a degree of political expediency in being associated with forest, even for farmers who fell forests to cultivate sun-loving crops. Walker (2005) goes so far as to refer to this phenomenon as the ‘arborealisation’ of conservation and development agendas. LOOKING FOR CLARITY ABOUT ‘FOREST’ IN THE PROFESSION OF FORESTRY Forestry can be defined as the science of cultivating forests (Webster 1983) or more broadly, such as in the definitions adopted by the Society of American Foresters and the International Union of Forest Research Organizations that include consideration of forest creation, use, and conservation (Helms 2002). Unfortunately, from its inception as a self-aware discipline in Europe, forestry has been 11 motivated by the oft-conflicting wishes of stakeholders who conceive of forests in quite different ways. From the perspective of many foresters and their official historians (e.g., Robinson 1975, Steen 1976), forestry developed as a utilitarian profession in response to society’s need to institute rational management of a rapidly degrading resource; that is, forest management for the general good of society. In bold contrast, a number of social historians and radical environmentalists portray the history of the forestry profession in decidedly less favorable light by focusing on its imperial, military, and industrial links (e.g., Shepherd 1975, Liphschitz & Biger 1998). The emphasis on cultivating forests, in general, and tree planting, in particular, in many definitions of forestry can be troublesome for both conservationists and foresters. For example, in evaluations of the environmental consequences of a country passing the ‘forest transition,’ the assumed equivalence of plantations and natural forests is fraught with environmental problems (Rudel et al. 2005). For the purposes of land-use mapping, at least intensive plantation management should be considered an agricultural activity. Ironically, the perceived need to plant trees can frustrate silviculturalists entrusted with management of areas already amply stocked with natural regeneration of the commercial species; protection and perhaps silvicultural release might be needed, but not replacement (e.g., Wadsworth & Zweede 2006, Peña-Claros et al. 2008a, b). Ultimately, trying to ferret out what is a ‘forest’ through consideration of the forestry profession leads only to the conclusion that forests are what foresters manage. In defense of the profession, the broad definition of forests endorsed by many foresters is in accord with the historical breadth of the term and is in keeping with society’s broad expectations of their roles as land stewards. ‘FOREST’ AS DEFINED BY INTERNATIONAL TREATIES AND NATIONAL LAWS The multitude of ways in which ‘forest’ is defined (Lund 2002) has myriad legal and practical implications in the contemporary world. The fundamental problem is that any definition that is appropriate for global (e.g., Bartholomé et al. 2002) and continental-scale land cover mapping (e.g., Eva et al. 2004), is not likely to be appropriate for monitoring biodiversity losses and intensities of forest use that do not qualify as deforestation but that result in substanital carbon fluxes. At such large scales, what is needed is a uniform set of basic parameters that can be mapped and monitored using readily available remote sensing technology. The vegetation classification system that the Food and Agriculture Organization of the United Nations developed for its longestablished global forest cover monitoring program (e.g., FAO 2001) provides the basics used by the Global Land Cover (Bartholomé et al. 2002) mapping project and by the United Nations Framework Convention on Climate Change (UNFCCC) for implementation of the Kyoto Protocol. The FAO’s basic definition of forest is an area of 4 0.5 ha with 4 10 percent tree canopy cover, with ‘trees’ defined as plants capable of growing 4 5 m tall (FAO 2001). The implementation guidelines of the Clean Development Mechanisms (CDM) of the Kyoto Protocol (i.e., the Marrakech SPECIAL SECTION 12 Putz and Redford Accords) are similar but allow each country to define ‘forest,’ at least to the extent of being allowed to choose the minimum treecrown cover required (10–30 percent), the minimum area of this cover (0.05–1.0 ha), and the minimum heights to which woody plants must be able to grow to be considered trees (2–5 m). At the next level of detail in their hierarchy of land cover types, the FAO distinguishes closed (4 40 percent canopy cover) and open (10–40 percent canopy cover) natural forests from plantations, but this distinction is often overlooked and is not reflected in CDM guidelines. National laws vary even more in regards to what is and what is not considered forest. In the Philippines, ‘forests’ do not legally occur on slopes 4 18 percent. In Spain, Finland, Norway, and Sweden, an area is not forested if it produces o 1 m3/ha/yr of timber whereas in Ireland, the minimum production for forest is 4 m3/ha/yr (Lund 2002). There is a clear need for widely accepted definitions of forest, deforestation, forest degradation, and forest restoration that are politically expedient but culturally sensitive, ecologically reasonable, and technologically feasible. The danger of overly simple definitions is that they can obscure substantial losses in what most people value as forest (Kleinn 2001). The needs for simple and globally applicable land cover classes notwithstanding, any definition based solely on canopy cover fails to recognize that forests are more than trees. An example of this problem is that following the rules of the Kyoto Protocol, up to 70–90 percent of the canopy of an initially closed-canopy forest could be destroyed and no deforestation would have occurred. Worse yet, even if the forest is entirely razed, as long as plants (including tree seedlings, palms, and bamboos) capable of growing to 4 2 or 5 m are present on 4 10–30 percent of the site will be allowed to regenerate, no deforestation would have occurred. Similarly, according to the FAO or under the guidelines of the Kyoto Protocol, old growth natural forests could be defaunated, clear-cut, or replaced by monoclonal stands of genetically modified exotic tree species grown for oil or fiber on 5–10 year rotations with no change in ‘forest’ cover (Niesten et al. 2002, Bekessy & Wintle 2008). Many policy-makers are cognizant of these sorts of threats to ecological integrity, but tropical biologists need to make sure that policy debates are well informed. FOREST AND ITS DERIVATIVES Although we realize that simple rules are needed for mapping and monitoring land cover at large spatial scales and recognize that the rules adopted were settled on only after extensive and continuing international debate, we are obviously uncomfortable with the way ‘forest’ is defined by global policy-makers and land cover mappers. To rectify this situation, we turned to our own discipline for clarity. Unfortunately, ecologists have never agreed on an explicit definition of ‘forest’ or of any other type of vegetation for that matter, and have often failed to differentiate between ‘potential’ and actual land cover types (e.g., Merriam 1898; Schimper 1903; Weaver & Clements 1929; Beard 1944, 1955; Richards 1952; Holdridge 1967; Daubenmire 1968; Walter 1971; Mueller-Dombois & Ellenberg 1974; Tracey 1982; but see Oliveira-Filho & Ratter 2002). Nevertheless, we find a fair degree of consensus in the way the world’s major ecosystem/vegetation/land cover types have been categorized. In particular, along the continuum from treeless to fully treed, the following vegetation types are typically designated (following Jennings et al. 2009): grasslands are dominated by graminoids ( = grasses and grass-like plants) with o 5 percent treecrown cover (note that we define a tree as a woody plant 4 5 m tall); savannas are graminoid dominated with scattered trees (5–20 percent treecrown cover); woodlands have graminoids in the understory and 20–40 percent treecrown cover; open forests have 40–70 percent treecrown cover; and, closed forests have 4 70 percent cover of treecrowns. Unfortunately, tropical ecosystems are not so easily classified; perhaps the single biggest failing of a system based solely on tree cover is lack of recognition of different sorts of scrub (e.g., cerrado, chaparral, fynbos, thicket, garrigue, mallee, maquis, and sand heath), ecosystems dominated by woody plants that exceed the lower height limit of 5 m but may never get much taller. There are also some shrub-dominated areas in the tropics, particularly near timberline and on thin, rocky, peaty, or heavy-metal-rich soils (Huber 1989), but they are not extensive. Surprisingly, ‘shrublands’ figure prominently in many modern land cover maps (e.g., Eva et al. 2004) and, for policy-informing and ecosystem state-change-predicting purposes, are often combined with grasslands and savannas into one category (e.g., Malhi et al. 2009). This change in map legends occurred at least partially because whereas most ecologists use the admittedly difficult to apply definition of ‘shrub’ as a multiple stemmed woody plant, for the FAO and its followers, shrubs are ‘woody perennial plants, generally 4 0.5 m and o 5 m in height at maturity without a definite crown’ (Schoene et al. 2007). Nonforest vegetation types can be ancient, rich in endemic species, and otherwise of great ecological value, but at least in a physiognomic sense, can also result from forest degradation. For example, whereas from a floristic perspective it is wrong to equate sparsely wooded cattle pastures with savannas, from physiognomic and remote-sensing perspectives, the two are difficult to distinguish. For this reason, we follow the established tradition of designating such clearly anthropogenic nonforest vegetation types as derived woodland, derived savanna, and derived scrub so as to not confuse them with structurally similar but generally much more species-rich communities (Richards 1952). There are widespread fears of savannas replacing forests in the Amazon Basin in particular and the tropics in general (Fairhead & Leach 1996, Cox et al. 2004, Nepstad et al. 2008, Malhi et al. 2009), but attention should also be given to the scrubs that figure prominently in the analyses of Beard (1955), Holdridge (1967), and Walter (1971). In these ecosystem classification systems, various sorts of scrub are expected to replace forest in lowland tropical areas where potential evapotranspiration exceeds precipitation; savanna is taken to be a ‘dysclimax’ that only develops where frequent fires or extreme pressure from browsing herbivores allow grasses to invade. We wonder, for example, whether, in addition to being concerned about ‘savannization,’ we should also address the threat of ‘scrubification.’ Perhaps the wide dissemination of highly productive and extremely flammable African C-4 pasture grasses throughout the Neotropics (Daubenmire 1972, Parsons SPECIAL SECTION Importance of Defining ‘Forest’ 1972) coupled with forest fragmentation, climate drying, and substantial increases in wildfire ignition by cattle-rearing and other people have tipped the balance toward savanna, but forest-scrub transitions also seem worthy of study. Complicating matters is the fact that, whereas some scrubs, woodlands, and savannas are recently anthropogenic, others are ancient and exceedingly rich in biodiversity and other ecological values. By denigrating these imperiled ecosystems as simply the by-products of forest degradation, we risk losing a great deal of conservation value. If we focus solely on forests but acknowledge that factors other than physiognomy or carbon stocks are to be considered, then it would help to clarify exactly what is at risk. While debates rage on over whether a particular forest is primary, pristine, intact, natural, virgin, or otherwise not anthropogenic (e.g., Clark 1996, Clement 1999), we need to start with an operational definition of ‘forest’ that reflects a diversity of ecological components, clarifies what is at risk, and promotes specification of the objectives of restoration efforts. Similarly, reference states need to be defined so that relative degrees of degradation can be compared among dissimilar forests (Tucker et al. 2008). An exemplary approach to defining a particular sort of reference state is provided by the U.S. Forest Service’s National Old-Growth Task Group. They define old growth as being ‘. . . distinguished by old trees and related structural attributes. Old growth encompasses the later stages of stand development that typically differ from earlier stages in a variety of characteristics that often include tree size, accumulations of large dead woody material, number of canopy layers, species composition, and ecosystem function.’ Recognizing that what constitutes ‘old’ varies from forest to forest, as do the attributes of old growth, the Task Force promoted publication of explicit old growth definitions for a variety of forest types in the United States. For example, old growth Douglas fir Pseudotsuga Menziesii in the Pacific Northwest of the United States is 4 175 years old, with the largest trees 4 100 cm dbh (diam. at 1.3 m), and with substantial stocks of coarse woody debris (Franklin et al. 1981). In stark contrast, old growth sand pine Pinus clausa in Florida can be as young as 45 years with the largest trees 4 26 cm dbh (Outcalt 1997). A similar approach is being used for the diverse suite of old growth vegetation types in Australia (Burgman 1996). Old growth woodlands, scrub, savanna, and grassland also deserve consideration, but here we restrict the discussion to forests and their derivatives. Although we use old growth forest as the basic reference state in our classification system (Fig. 1), what is of fundamental importance is clarity about what is being lost or gained. We acknowledge that if conservation efforts are to be successful, reference state selection should reflect the wishes and concepts of local people (e.g., Moyer et al. 2008) and not be imposed by scientists, however well intentioned. Nonetheless, we do not address this fundamental consideration other than to point out that where local and extra-local stakeholder visions differ, appropriate compromises need to be fairly negotiated. At least in the biophysical sense, restoration ecologists are well aware of the importance of identifying reference states (e.g., Egan & Howell 2001, but see Pickett & Parker 1995) even when prime ecosystem examples no longer exist (Dettman & Mabry 2008) and when the climate and other influential factors are 13 changing (Fulé 2008). In contrast, reference states are seldom made explicit in discussions of tropical forest degradation, deforestation, and recovery; designating these states becomes more challenging with the near disappearance of some formerly extensive forest types (Ashton 2008). Old growth forests that have lost their defining compositional and structural attributes due to wildfires (or the converse in firemaintained ecosystems), invasion by exotic species, over hunting, or other substantial human interventions are classified as degraded forest; other researchers have used the term ‘nonintact’ and a variety of other adjectives for similar state changes (Clement 1999, Mollicone et al. 2007). Uncontrolled, repeated-entry logging with attendant hunting followed by fire is a common sequence of forest degrading processes in many parts of the tropics (Nepstad et al. 1999, Cochrane 2003). Defaunation by over-hunting is another way in which old growth forest is lost; we classify the resulting ‘empty forests’ (Redford 1992, Terborgh et al. 2008) as degraded forest. In this admittedly coarse classification system, the ‘novel ecosystems’ that develop with incorporation of exotic species or after massive biogeochemical changes would also be considered degraded forest if they retain the defining characteristics of forest. Forests that are purposefully domesticated for production of timber and nontimber forest products should be referred to as managed forests; the ‘semi-natural forests’ of the Forest Stewardship Council (FSC) (2009) would presumably be included in this category. We recognize that this designation suffers insofar as one person’s management is another’s degradation, that many forests formerly considered pristine show vestiges of historical human interventions, and that considerable power derives from the right to define these states (Tsing 2005). Furthermore, the extent of management-induced modification depends on whether maximization of production is the sole objective of management and on the silvicultural treatments employed. And finally, modern commercial production forestry differs substantially from the range of indigenous forest domestication processes that led Clement (1999) to differentiate among what he referred to as pristine, promoted, managed, cultivated, and swidden/fallow landscapes. In our more simplistic approach, the defining differences in structure and composition between managed and old growth forest often include reductions in the densities of adults of commercial species and, where logging has occurred, increases in the densities of lightdemanding plant species. Forests that develop after complete deforestation should be referred to as secondary forests. Although some researchers do not distinguish between secondary and degraded forest, we believe that these types of forest are different enough in structure, composition, dynamics, and management options to warrant distinction. Secondary forests that develop on land used for intensive agriculture and pastures, for example, regenerate mostly from seeds that are either dispersed in from nearby remnant forest or, to a lesser extent, germinate from buried dormant seeds. In contrast, regeneration after logging in managed or degraded forests is typically dominated by vegetative recovery of plants that remained on site through the episode of damage. Furthermore, although secondary forests rapidly develop some of the structural, compositional, and functional SPECIAL SECTION 14 Putz and Redford FIGURE 1. Ecological state changes starting from the reference condition of tropical old growth forest. Only the principal drivers are included (in hexagons) and not all possible transitions away from the reference condition are depicted. Back transitions that result from natural succession as well as afforestation, reforestation, forest management, and other restoration activities are not indicated to reduce figure clutter. characteristics of old growth forest (Chazdon 2003), other features recover only after centuries if ever (Clark 1996). As mentioned above, to help avoid the major losses in biodiversity that result from converting forests into plantations (e.g., Barlow et al. 2007, Fitzherbert et al. 2008), these two categories should not be combined. The Dictionary of Forestry (Helms 1998) defines plantation as ‘a stand composed primarily of trees established by planting or artificial seeding.’ Using this broad definition, plantations include a tremendous range of management intensities, structures, and compositions. At one end of this continuum are industrial tree farms comprised of genetically modified monoclonal exotic tree species planted after mechanical removal or broadcast herbicide treatment of all competing vegetation and clear-cut at 5–25 yr intervals. At the same end of this continuum, we place oil palm plantations, intensively managed rubber estates, and other types of tree farms. Although these stands of perennials may somewhat resemble forests in ecosystem functions such as sequestration of carbon, nutrient cycling, and hydrology, they are very different in structure and often completely different in composition and, hence, we call them plantations not ‘planted forest’ and include them among other agricultural land-uses. At the other end of the continuum of management intensity from intensively managed monocultures of exotic tree species are rustic coffee and cacao agroforests (Bhagwat et al. 2008), ‘forest gardens’ in Indonesia (Padoch & Peters 1993), and the substantially enriched, promoted, and otherwise modified ‘seminatural’ forests of the Amazon (Roosevelt 1980, Posey 1984, Balee 1994, Clement 1999, Lentz 2000). Some of these managed communities are so ‘natural’ in structure and composition that they are often mistaken for old growth forest and in many cases should be classified as managed forest. Also complicating differentiation between plantations and managed forests are planted stands of native trees with more-or-less intact understories of native groundcovers. Examples of this intermediate condition include the degraded forests in Malaysia that are gradually converted SPECIAL SECTION Importance of Defining ‘Forest’ into plantations of native dipterocarps by enrichment planting (Moura Costa et al. 1996) and the intensively managed groves of Euterpe oleraceae palms near the mouth of the Amazon (Brondizio et al. 1994). The issue of whether plantations should be considered a type of forest is politically quite contentious. The World Rainforest Movement (http://www.wrm.org.uy) and the Dogwood Alliance (http://www.dogwoodalliance.org), for example, have mounted substantial campaigns against the FSC’s certification of plantation management. Although the FSC will not certify plantations that replaced forests after 1994, it is blamed for contributing to the confusion over what is and what is not ‘forest,’ thereby inadvertently contributing to the loss of natural ecosystems. Narrowly defining ‘forests’ and differentiating them from woodlands, savanna, shrublands, and scrub may make ecological sense but it may also cause these nonforest ecosystems to be further threatened. The arborealization of global conservation agendas can cause conflicts when nontree values, like wildlife, and naturally treescarce ecosystems are in jeopardy. This focus on trees derives in part from recognition of the need to consider the fate of biomass carbon in efforts to mitigate the climate-changing effects of fossil fuel combustion. Nevertheless, ecosystems other than forests sequester carbon, and a ‘forest’ definition that may suffice from carbon and remote sensing perspectives is not likely to satisfy concerns about biodiversity, cultural amenities, and other ecosystem services. DEFINING DEFORESTATION AND FOREST DEGRADATION Although the attention paid to deforestation in the tropics is well justified, it is worrisome that the more extensive and often more insidious processes of forest degradation are often overlooked. One reason for this neglect is that ‘degradation’ denotes loss of values that are subjective and thus often ignored by scientists. Another reason for degradation’s disregard is that it is more difficult to detect using remote sensing techniques. Furthermore, while deforestation can be portrayed as a binary variable (deforested or not), degradation occurs on continua that pass through numerous nonorthogonal dimensions and follow trajectories affected by thresholds and other nonlinearities. Familiar forms of tropical forest degradation include nonsustainable (but still ‘selective’) harvesting of timber and nontimber forest products, over-hunting, and slowmoving low intensity understory fires that kill small trees and shorten the life expectancies of large ones. Improved access promotes both deforestation and forest degradation, but the latter often proceeds much farther beyond the reach of roads or the law. For example, given the extremely high price per gram of gaharu Aquilaria malaccensis wood incense, we doubt there is any place on the island of Borneo where trees of this species are beyond the reach of harvesters. Similarly, bush meat hunters will walk great distances for game, which renders it challenging to maintain populations of large, charismatic, edible, or otherwise marketable species anywhere within 10–50 km of the nearest settlement. And when the hunted species are migratory or are drawn to saltlicks or the fresh foliage on hunted-out roadsides, 15 even stationary hunters can defaunate huge areas (Robinson & Bennett 2004, Nasi et al. 2008). While much attention has been paid to the deforestation that results from perverse policies, such as those that require forest clearing before land titles are granted (Williams 2003), under a range of circumstances, forest degradation is likely in places where outright deforestation might otherwise be expected. For example, if remote sensing is used for official forest monitoring and if regulations prohibiting deforestation are enforced, forest exploiters may choose to restrict themselves to degradation rather than outright deforestation. Similarly, forest exploiters who are also guerillas, smugglers, and drug plant cultivators might stop short of radically opening the canopy and thus exposing their activities to aerial detection. Finally, where land-use intensification is limited by access to capital, forest degradation is more likely than deforestation until better capitalized actors enter the area or the costs of conversion go down, such as when access improves as a result of road building or paving (Chomitz et al. 2007). The Kyoto Protocol provides no provisions for reducing emissions of carbon dioxide and other atmospheric heat-trapping gases by avoiding deforestation or forest degradation but does provide carbon credits for ‘reforestation’ and ‘afforestation’ of areas that were not forest covered on 1 January 1990 or 1 January 1940, respectively. One of the real-world consequences of the political process that resulted in this international agreement is that countries that selected a higher treecrown cover threshold (i.e., 30% vs. 10%) for defining forest generally have substantially more land eligible for carbon credits from tree planting (Verchot et al. 2007, Zomer et al. 2008). What we find worrisome is that under these guidelines, carbon funding could be made available for replacing species-rich grasslands, savannas, and woodlands with trees or deep rooted plants that sequester more carbon than the native ecosystem (Fisher et al. 1994). Hopefully, the systems used in the voluntary carbon markets to assure that forest carbon is sequestered in socially and ecologically sound manners (e.g., Hamilton et al. 2008) will be adopted by the regulated carbon markets expected to emerge from international climate change convention under negotiation. With the Kyoto Protocol set to expire in 2012, the UNFCCC is now in the process of developing a new climate change agreement. Recognizing that the fate of tropical forest carbon cannot be disregarded if cataclysmic climate change is to be averted, negotiators of the new convention are discussing the ‘reduced emissions from deforestation and forest degradation’ (REDD) option (Gibbs et al. 2007). Cost-effectiveness has drawn attention to REDD (Stern 2006, Kinderman et al. 2008), but most emphasis in the debates has been on deforestation and not on degradation. We are concerned that the second ‘D’ in this now familiar acronym is often dropped altogether (e.g., Hall 2008), mentioned but then disregarded (Gibbs et al. 2007), or is interpreted as standing for ‘developing countries’ instead of ‘degradation’ (UNFCCC 2006, Putz et al. 2008). Whereas degradation is often obvious from the ground, it is more difficult to detect from space. Fortunately, recent improvements in remote sensing technologies are increasing our ability to detect the effects of selective logging on canopy closure (Asner et al. SPECIAL SECTION 16 Putz and Redford 2005, Oliveira et al. 2007, Broadbent et al. 2008, Duveiller et al. 2008, Palace et al. 2008), the effects of understory fires (Alencar et al. 2006), and even the understory invasion of exotic species (Asner & Vitousek 2005, Asner et al. 2008). Nevertheless, other sorts of forest degradation are and will remain invisible from satellites (e.g., over-hunting; Peres et al. 2006) and, thus, ground-based studies will continue to be needed if the extensive, pervasive, and pernicious impacts of forest degradation are to be avoided. If some of the attention of environmental policy-makers can be shifted from deforestation to forest degradation, the differences between the two processes will need to be clarified (Southworth et al. in press). If degradation is defined solely in terms of reductions in canopy cover, then degradation proceeds up to the threshold of deforestation (e.g., 10–30% treecrown cover, as set by Marrakech Accords), but could just as well be based on the limitations of the remote sensing technology utilized. Unfortunately, even this simplified portrayal of the conversion process fails to distinguish between forest degradation and forest management. For example, what looks like degradation from space, as defined as canopy losses that do not constitute deforestation, might intentionally result from silvicultural treatments applied to promote regeneration of lightdemanding species. Similarly, removal of invasive exotic and nuisance native trees is often a step towards ecosystem restoration and does not constitute degradation (Condon & Putz 2007). FOREST TRANSITIONS In the ecosystem classification system we propose, old growth forests that lose their defining attributes (e.g., ancient trees, fauna, and coarse woody debris) through logging, market hunting, wildfires, or invasion by exotic species, become degraded forest (Fig. 1). In contrast, where people purposefully change forest structure and composition through silvicultural treatments to favor economically valuable species, the result is managed forest. Where forest managers attempt to mimic natural disturbance regimes or where they explicitly manage for old growth characteristics (Landres et al. 1999, O’Hara 2001), the resemblance between managed forest and old growth forest can be substantial. Boundaries of managed forest are similarly difficult to set because the degree of domestication varies so greatly (Clement 1999). Contrast, for example, a forest that was managed by stone-tool wielding hunter–gatherers for the production of medicinal plants and other nontimber forest products from native species (Balee 1994) with a forest silviculturally managed for commercial timber through heavy logging, liana cutting, and girdling of all noncommercial trees (e.g., the Malayan Uniform System; see Lee et al. 1998 for an assessments of such an area 34 years after felling and treatment). But even where human interventions are intensive, such as in species-rich and multi-storied agroforests dominated by native trees species (e.g., Michon et al. 1986), many of the structural, floristic, and functional features of old growth forest are maintained (but see Bhagwat et al. 2008). In response to uncontrolled multiple entry logging followed by fire and other perturbations, ecosystem ‘phase’ shifts are likely from old growth forest to a variety of physiognomically and floristically distinctive states including derived scrub, derived woodland, and derived savanna, depending on canopy cover and tree stature (Fig. 1). Which of these derived vegetation types develops depends mostly on the fire regime, which is in turn mostly determined by the presence and abundance of fire-favoring grasses and social factors. In particular, in response to severe disturbances or climate drying, where grasses are scarce, forest is most likely to be replaced by derived scrub rather than the fire-dependent derived woodland or derived savanna. The fates of deforested areas left to regenerate also vary greatly with the type, duration, and spatial extent of nonforest land-uses. Where land uses were of low intensity and short duration, such as in the small clearings of swidden agriculturalists, natural regeneration can be rapid from resprouting, germination of seeds from the buried seed bank, or establishment from seeds dispersed in from nearby forest remnants. In contrast, large and hard-used pastures and plowed lands develop only slowly into very different sorts of secondary forests or not at all if fires recur. These secondary forests may become old growth after decades or centuries of protection, unless they are colonized by exotic species or if forest succession is prevented by climate change. They can also be silviculturally treated in ways that speed the transition into old growth, managed for any of a variety of forest products and services, or degraded by logging or repeated fires to the extent that they become derived woodland, derived scrub, or even derived savanna. Alternatively, if planted with either native or exotic tree species, deforested areas can become plantations or even urban forests, an important category we have not discussed. Finally, plantations that are abandoned or otherwise not intensively managed for fiber, fuel, oil, latex, or other products are generally colonized by native and exotic species, which eventually convert them into secondary forests. Unfortunately, despite the flurry of publications on using plantations to facilitate forest succession on degraded sites in the tropics (e.g., Parrotta 1992, Parrotta & Turnbull 1997), it is not clear that this phenomenon is widespread. Furthermore, many secondary forests are essentially forest fallows subject to reclearing when prices for agricultural commodities rise (Rudel et al. 2002). Finally, recovery towards old growth forest or any other static reference state can be permanently deflected by climate change or other alterations in abiotic conditions, species extinctions, and the existence of persistent exotic species. CONCLUSIONS Vegetation classification systems, like the one we present, can serve to foster communication but admittedly fail to capture the fluidity of ‘forest’ and other ecosystem types both in nature and as social constructs. This fluidity is to be expected given the extent to which ‘forest’ is a term used for political and social gains. It is also expected given the range of ecosystem types being considered, their propensity for change, and the many ways they are perceived, remembered, and valued. Clearly, confusion over what is and what is not forest is rooted in substantial cultural ambivalence. As revealed by its etymology, ‘forest’ has historically been outside, beyond the walls, and at the frontiers of civilization. Indeed, civilization is often portrayed as pitting itself against forests (but see Frazer 1890). But while forests have always harbored outlaws (some of whom stood for justice), SPECIAL SECTION Importance of Defining ‘Forest’ wild men, wild beasts, and the danger of disorientation, they have also been sources of spiritual enlightenment and tranquility as well as refuges for the downtrodden (Harrison 1992). Furthermore, at least since the advent of scientific forestry in Germany in the 18th Century, forests have also been perceived as sources of raw materials for society. Lack of clarity in descriptions of historical ecosystems becomes more than an academic dilemma when reference states for ecosystem restoration are selected. Were the sacred cedar groves that King Gilgamesh of Sumeria reputedly destroyed 4000 years ago (Harrison 1992) forests or woodlands? Could a Pre-Columbian North American squirrel have traveled from the Atlantic seaboard to the Mississippi River without touching the ground, or did Amerindian burning and farming preclude this possibility (Cronon 1983)? Similarly, was the largest remaining tract of ‘pristine’ forest in Central America a patchwork of maize fields when visited by Balboa in the early 1500 s (Bush & Colinvaux 1994)? Mounting archeological and ecological evidence of prior human modification has stimulated some researchers to cast doubts about the virginity of even remote forests in the Amazonian Hylea (Lentz 2000, Heckenberger et al. 2008), but more recent assessments have suggested that while human influences were substantial, they were also somewhat localized (Bush & Silman 2007). But while selection of historically appropriate reference states is an acknowledged challenge, with rapid rates of global change in climate and species distributions, it is not clear how much history should guide conservation and restoration. Lack of consensus about what is and what is not ‘forest’ contributes to the haze in which ecological destruction continues unabated. With implementation of market-based approaches to forest protection, clarification of terms used to describe different ecosystem states is a prerequisite for effective communication, policymaking, and conservation. It is certainly more than semantic when forests are converted into plantations in the name of climate change mitigation, and massive deforestation and forest degradation go unrecorded because of the way ‘forest’ is defined. Furthermore, the frequency and severity of conflicts between interventions motivated by the global conventions on biodiversity and climate change should decline when it is clear what is at stake (e.g., old growth forest or derived scrub). Finally, in all manners of human discourse, forests will remain something of a social construct, but one that should be firmly rooted in ecosystem structure and composition. ACKNOWLEDGMENTS We cannot thank all of the people who helped shape our thinking about this topic but we can at least acknowledge those who suggested improvements on earlier drafts of the manuscript including V. Medjibe, S. Murphy, A. Shenkin, J. Ash, K. Didier, P. Zuidema, C. Romero, J. Veldman, P. Brando, R. Chazdon, and an anonymous reviewer. Participation in a workshop on ‘Land Use Transitions in the Tropics’ at Rutgers University provided the final impetus for preparing this paper. 17 LITERATURE CITED AGNOLETTI, M., AND S. ANDERSON (Eds.). 2000. Forest history: International studies on socio-economic and forest ecosystem change. CAB International Publishing, Oxford, UK. ALENCAR, A., D. NEPSTAD, AND M. DEL C. DIAZ. 2006. Forest understory fire in the Brazilian Amazon in ENSO and non-ENSO years: Area burned and committed carbon emissions. Earth Interact. 10: 1–17. ASHTON, P. S. 2008. Changing values of Malaysian forests: The challenge of biodiversity and its sustainable management. J. Trop. For. Sci. 20: 282–291. ASNER, G. P., M. O. JONES, R. E. MARTIN, D. E. KNAPP, AND R. F. HUGHES. 2008. Remote sensing of native and invasive species in Hawaiian forests. Remote Sens. Environ. 112: 1912–1926. ASNER, G. P., D. E. KNAPP, E. N. BROADBENT, P. J. C. OLIVEIRA, M. KELLER, AND J. N. SILVA. 2005. Selective logging in the Brazilian Amazon. Science 310: 480–482. ASNER, G. P., AND P. M. VITOUSEK. 2005. Remote analysis of biological invasion and biogeochemical change. Proc. Nat. Acad. Sci. USA 102: 4383–4386. BALEE, W. 1994. Footprints of the forest. Columbia University Press, New York, New York. BARLOW, J., T. A. GARDNER, I. S. ARAUJO, T. C. ÁVILA-PIRES, A. B. BONALDO, J. E. COSTA, M. C. ESPOSITO, L. V. FERREIRA, J. HAWES, M. I. M. HERNANDEZ, M. S. HOOGMOED, R. N. LEITE, N. F. LO-MAN-HUNG, J. R. MALCOLM, M. B. MARTINS, L. A. M. MESTRE, R. MIRANDA-SANTOS, A. L. NUNES-GUTJAHR, W. L. OVERAL, L. PARRY, S. L. PETERS, M. A. RIBEIROJUNIOR, M. N. F. DA SILVA, C. DA SILVA MOTTA AND C. A. PERES. 2007. Quantifying the biodiversity value of tropical primary, secondary, and plantation forests. Proc. Nat. Acad. Sci. USA 104: 18555–18560. BARTHOLOMÉ, E., A. S. BELWARD, F. ACHARD, S. BARTALEV, C. CARMONAMORENO, H. EVA, S. FRITZ, J-M. GREGOIRE, P. MAYAUX, AND H-J. STIBIG. 2002. GLC 2000: Global land cover mapping for the year 2000. European Commission Joint Research Centre, Ispra, Italy. BEARD, J. S. 1944. Climax vegetation in tropical America. Ecology 25: 127–158. BEARD, J. S. 1955. The classification of tropical American vegetation types. Ecology 36: 89–100. BEKESSY, S. A., AND B. A. WINTLE. 2008. Using carbon investment to grow the biodiversity bank. Conserv. Biol. 22: 510–513. BHAGWAT, S. A., K. J. WILLIS, J. B. BIRKS, AND R. J. WHITTAKER. 2008. Agroforestry: A refuge for tropical biodiversity? Trends Ecol. Evol. 23: 261–267. BROADBENT, E. N., G. P. ASNER, M. PEÑA-CLAROS, M. PALACE, AND M. SORIANO. 2008. Spatial partitioning of biomass and diversity in a lowland Bolivian forest: Linking field and remote sensing measurements. For. Ecol. Manage. 255: 2602–2616. BRONDIZIO, E. S., E. F. MORAN, P. MAUSEL, AND Y. WU. 1994. Land use change in the Amazon estuary: Patterns of caboclo settlement and landscape management. Human Ecol. 22: 249–278. BROSIUS, J. P. 1997. Endangered forest, endangered people: Environmentalist representations of indigenous knowledge. Human Ecol. 25: 47–69. BURGMAN, M. A. 1996. Characterization and delineation of the eucalypt oldgrowth forest estate in Australia: A review. For. Ecol. Manage. 83: 149–161. BUSH, M. B., AND P. A. COLINVAUX. 1994. A paleoecological perspective of tropical forest disturbance: Records from Darien, Panama. Ecology 75: 1761–1768. BUSH, M. B., AND M. R. SILMAN. 2007. Amazonian exploitation revisited: Ecological asymmetry and the policy pendulum. Front. Ecol. Environ. 5: 457–465. CHAZDON, R. L. 2003. Tropical forest recovery: Legacies of human impact and natural disturbances. Persp. Plant Ecol. Evol. Syst.: 6: 51–71. CHOMITZ, K. M., P. BUYS, G. DE LUCA, T. S. THOMAS, AND S. WERTZKANOUNNIKOFF. 2007. At loggerheads? Agricultural expansion, poverty SPECIAL SECTION 18 Putz and Redford reduction, and environment in the tropical forests. The World Bank, Washington, DC. CLARK, D. B. 1996. Abolishing virginity. J. Trop. Ecol. 12: 735–739. CLEMENT, C. R. 1999. 1492 and the loss of Amazonian crop genetic resources. I. The relation between domestication and human population decline. Econ. Bot. 53: 188–202. COCHRANE, M. A. 2003. Fire science for rainforests. Nature 421: 913–919. CONDON, B. M., AND F. E. PUTZ. 2007. Countering the broadleaf invasion: Financial and carbon consequences of removing hardwoods during longleaf pine savanna restoration. Rest. Ecol. 15: 296–303. COX, P. M., R. A. BETTS, M. COLLINS, P. P. HARRIS, C. HUNTINGFORD, AND C. D. JONES. 2004. Amazonian forest dieback under climate-carbon cycle projections for the 21st century. Theor. Appl. Climatol. 78: 137–156. CRONON, W. 1983. Changes in the land: Indians, colonists, and the ecology of New England. Hill and Wang, New York, New York. DAUBENMIRE, R. 1972. Ecology of Hyparrehnia rufa (Nees) in derived savanna in north-western Costa Rica. J. Appl. Ecol. 9: 11–23. DAUBENMIRE, R. F. 1968. Plant communities: A textbook of plant sociology. Harper and Row, New York, New York. DAWKINS, H. C., AND M. S. PHILIP. 1998. Tropical moist forest silviculture and management: A history of success and failure. CAB International, Oxford, UK. DETTMAN, C. L., AND C. M. MABRY. 2008. Lessons learned about research and management: A case study from a Midwest lowland savanna, U.S.A. Rest. Ecol. 16: 532–541. DUVEILLER, G., P. DEFOURNY, B. DESCLEE, AND P. MAYAUX. 2008. Deforestation in Central Africa: Estimates at regional, national and landscape levels by advanced processing of systematically-distributed Landsat extracts. Remote Sens. Environ. 112: 1969–1981. EGAN, D., AND E. A. HOWELL (Eds.). 2001. The historical ecology handbook: A restorationist’s guide to reference ecosystems. Island Press, Washington, DC. EVA, H. D., A. S. BELWARD, E. E. DE MIRANDA, C. M. DI BELLA, V. GOND, O. HUBER, S. JONES, M. SGRENZAROLI, AND S. FRITZ. 2004. A land cover map of South America. Global Change Biol. 10: 731–744. FAIRHEAD, J., AND M. LEACH. 1996. Misreading the African landscape: Society and ecology in a forest-savanna mosaic. Cambridge University Press, Cambridge, UK. FAO. 2001. Global Forest Resources Assessment 2000. FAO Forestry Paper 140. FARLEY, K. A. 2007. Grassland to tree plantations: Forest transition in the Andes of Ecuador. Ann. Ass. Am. Geogr. 97: 755–771. FISHER, M. J., I. M. RAO, M. A. AYARZA, C. E. LASCANO, J. I. SANZ, R. J. THOMAS, AND R. R. VERA. 1994. Carbon storage by introduced deep-rooted grasses in the South American savannas. Nature 371: 236–238. FITZHERBERT, E. B., M. J. STUEBIG, A. MOREL, F. DANIELSEN, C. A. BRUHL, P. F. DONALD, AND B. PHALAN. 2008. How will oil palm expansion affect biodiversity? Trends Ecol. Evol. 23: 538–545. FOLEY, J. A., G. P. ASNER, M. H. COSTA, M. T. COE, R. DEFRIES, H. K. GIBBS, E. A. HOWARD, S. OLSON, J. PATZ, N. RAMANKUTTY, AND P. SNYDER. 2007. Amazon revealed: Forest degradation and loss of ecosystem goods and services in the Amazon Basin. Front. Ecol. Envir. 5: 25–32. FOREST STEWARDSHIP COUNCIL. 2009. Draft 6.1 FSC US national forest management standard. Available at http://www.fscus.org/images/documents/ standards/revision%20process%20fall%2008/finaldraft.pdf (accessed March 23, 2009). FRANKLIN, J. F., K. CROMACK JR., W. DENISON, A. MCKEE, C. MASER, J. SEDELL, F. SWANSON, AND G. JUDAY. 1981 Ecological characteristics of oldgrowth Douglas-fir forest. USDA Forest Service GTR PNW 118. FRAZER, J. G. 1890. The golden bough. Macmillan, London, UK. FULÉ, P. Z. 2008. Does it make sense to restore wildland fire in changing climate? Rest. Ecol. 16: 526–531. GIBBS, H. K., S. BROWN, J. O. NILES, AND J. A. FOLEY. 2007. Monitoring and estimating tropical forest carbon stocks: Making REDD a reality. Environ. Res. Letters 2: 045023. HALL, A. 2008. Better RED than dead: Paying the people for environmental services in Amazonia. Phil. Trans. Royal Soc. B 363: 1925–1932. HAMILTON, K., R. BAYON, AND A. HAWN. 2008. Carving a niche for forests in the voluntary carbon markets. In C. Strecht, R. O’Sullivan, T. JansonSmith, and R. Tarasofsky (Eds.). Climate change and forests: Emerging policy and market opportunities, pp. 292–307. Chatham House, London, UK. HARRISON, R. P. 1992. Forests: The shadow of civilization. University of Chicago Press, Chicago, Illinois. HECKENBERGER, M. J., J. C. RUSSELL, C. FAUSTO, J. R. TONEY, M. J. SCHMIDT, E. PEREIRA, B. FRANCHETTO, AND A. KUIKURO. 2008. Pre-Columbian urbanism, anthropogenic landscapes, and the future of the Amazon. Science 321: 1214–1217. HELMS, J. A. (Ed.). 1998. The dictionary of forestry. Society of American Foresters, Bethesda, Maryland. HELMS, J. A. 2002. Forest, forestry, forester: What do these terms mean? J. For. 100: 15–19. HOLDRIDGE, L. R. 1967. Life zone ecology. Tropical Science Center, San Jose, Costa Rica. HUBER, O. 1989. Shrublands of the Venezuelan Guayana. In L. B. HolmNielsen, I. C. Nielsen, and H. Baslev (Eds.). Tropical forests. Botanical dynamics, speciation and diversity, pp. 271–285. Academic Press, London, UK. JENNINGS, M., D. FABER-LANGENDOEN, O. L. LOUCKS, R. K. PEET, AND D. ROBERTS. 2009. Standards for associations and alliances of the U.S. National Vegetation Classification. Ecol. Monogr. 79: 173–199. KINDERMAN, G., M. OBESSTEINER, B. SOHNGEN, J. SATHAYE, K. ANDRASKO, E. RAMETSTEINER, B. SCHLAMADINGER, S. WUNDER, AND R. BEACH. 2008. Global cost estimates of reducing carbon emissions through avoided deforestation. Proc. Nat. Acad. Sci. USA 105: 10302–10307. KLEINN, C. 2001. A cautionary note on the minimum crown cover criterion in forest definitions. Can. J. For. Res. 31: 350–356. LANDRES, P. B., P. MORGAN, AND F. J. SWANSON. 1999. Overview of the use of natural variability concepts in managing ecological systems. Ecol. Appl. 9: 1179–1188. LEE, S. S., Y. M. DAN, I. D. GAULD, AND J. BISHOP. 1998. Conservation, management and development of forest resources. Forest Research Institute of Malaysia, Kepong, Malaysia. LENTZ, D. L. (Ed.). 2000. Imperfect balance. Landscape transformations in the Precolumbian Americas. Columbia University Press, New York, New York. LIPHSCHITZ, N., AND G. BIGER. 1998. Afforestation policy of the Zionist movement in Palestine 1895-1948. In C. Watkins (Ed.). European woods and forests: Studies in cultural history, pp. 165–180. CAB International, Oxford, UK. LUND, H. G. 2002. When is a forest not a forest? J. For. 100: 21–28. MALHI, Y., L. E. O. C. ARAGAO, D. GALBRAITH, C. HUNTINGFORD, R. FISHER, P. ZELAZOWSKI, S. SITCH, C. MCSWEENEY, AND P. MEIR. 2009. Exploring the likelihood and mechanism of climate-change-induced dieback of the Amazon rainforest. Proc. Nat. Acad. Sci. USA. doi: 10.1073/pnas. 0804619106. MATHER, A. 1990. Global forest resources. Bellhaven Press, London, UK. MERRIAM, C. H. 1898. Life zones and crop zones of the United States. USDA Division of Biological Survey, Bulletin 10: 1–79. MICHON, G., F. MARY, AND J. BOMPARD. 1986. Multistoried agroforestry garden systems in West Sumatra. Agrofor. Sys. 4: 315–338. MOLLICONE, D., F. ACHARD, S. FEDERICI, H. D. EVA, G. GRASSI, A. BELWARD, F. RAES, G. SEUFERT, H. J. STIBIG, G. MATTEUCCI, AND E. D. SCHULZE. 2007. An incentive mechanism for reducing emissions from conversion of intact and non-intact forests. Clim. Change 83: 477–493. MOURA COSTA, P., S. W. YAP, C. L. ONG, A. GANING, R. NUSSBAUM, AND T. MOJIUN. 1996. Large-scale enrichment planting with dipterocarps as an alternative for carbon-offset methods and preliminary results. In S. Appanah and K. C. Khoo (Eds.). Proceedings of the fifth round table conference on dipterocarps, pp. 386–396. Forest Research Institute of Malaysia, Kepong, Malaysia. SPECIAL SECTION Importance of Defining ‘Forest’ MOYER, J. M., R. J. OWEN, AND P. N. DUINKER. 2008. Forest values: A framework for old-growth with implications for other forest conditions. The Open Forest Science Journal 1: 27–36. MUELLER-DOMBOIS, D., AND H. ELLENBERG. 1974. Aims and methods of vegetation ecology. Wiley, New York, New York. NASI, R., D. BROWN, D. WILKIE, E. BENNETT, C. TUTIN, G. VAN TOL, AND T. CHRISTOPHERSEN. 2008. Conservation and use of wildlife-based resources: the bushmeat crisis. Secretariat of the Convention on Biological Diversity, Montreal, and Center for International Forestry Research, Bogor. Technical Series no. 33. NEPSTAD, D. C., C. M. STICKLER, B. SOARES-FILHO, AND F. MERRY. 2008. Interactions among Amazon land use, forests and climate: Prospects for a near-term forest tipping point. Phil. Trans. Royal Soc. B 363: 1737–1746. NEPSTAD, D. C., A. VERISSIMO, A. ALENCAR, C. NOBRE, E. LIMA, P. LEFEBVRE, P. SCHLESINGER, C. POTTER, P. MOUTINHO, E. MENDOZA, M. COCHRANE, AND V. BROOKS. 1999. Large-scale impoverishment of Amazonian forests by logging and fire. Nature 398: 505–508. NIESTEN, E., P. C. FRUMHOFF, M. MANION, AND J. J. HARDNER. 2002. Designing a carbon market that protects forests in developing countries. Philos. Trans. R. Soc. Lond. Ser. A 360: 1875–1888. O’HARA, K. L. 2001. The silviculture of transformation—a commentary. For. Ecol. Manage. 151: 81–86. OLIVEIRA, P. J., G. P. ASNER, D. E. KNAPP, A. ALMEYDA, R. GALVÁN-GILDMEISTER, S. KEENE, R. F. RAYBIN, AND R. C. SMITH. 2007. Land-use allocation protects the Peruvian Amazon. Science 317: 1233–1236. OLIVEIRA-FILHO, A. T., AND J. A. RATTER. 2002. Vegetation physiognomies and woody flora of the cerrado biome. In P. S. Oliveira and R. J. Marquis (Eds.). The cerrados of Brazil: Ecology and natural history of a neotropical savanna, pp. 91–120. Columbia University Press, New York, New York. OUTCALT, K. W. 1997. An old-growth definition for sand pine forests. USDA Forest Service GTR SRS-12. PADOCH, C., AND C. M. PETERS. 1993. Managed forest gardens in West Kalimantan, Indonesia. In C. S. Potter, J. I. Cohen, and D. Janczewski (Eds.). Perspectives on biodiversity: Case studies of genetic resource conservation and development, pp. 167–176. American Association for the Advancement of Sciences Press, Washington, DC. PALACE, M., M. KELLER, G. P. ASNER, S. HOGEN, AND B. BRASWELL. 2008. Amazon forest structure from IKONOS satellite data and the automated characterization of forest canopy properties. Biotropica 40: 141–150. PARROTTA, J. A. 1992. The role of plantation forests in rehabilitating degraded tropical ecosystems. Agric. Ecosys. Environ. 41: 115–133. PARROTTA, J. A., AND J. W. TURNBULL. 1997. Catalyzing native forest regeneration on degraded tropical lands. For. Ecol. Manage. 99: 1–299. PARSONS, J. J. 1972. Spread of African pasture grasses to the American tropics. J. Range Manage. 25: 12–17. PELUSO, N. L. 1992. Rich forests, poor people. University of California Press, Berkeley, California. PEÑA-CLAROS, M., E. M. PETERS, M. J. JUSTINIANO, F. BONGERS, G. M. BLATE, T. S. FREDERICKSEN, AND F. E. PUTZ. 2008b. Regeneration of commercial trees species following silvicultural treatments in a moist tropical forest. For. Ecol. Manage. 255: 1283–1293. PEÑA-CLAROS, M. L., T. S. FREDERICKSEN, A. ALARCON, G. M. BLATE, U. CHOQUE, C. LEAÑO, B. MOSTACEDO, W. PARIONA, Z. VILLEGAS, AND F. E. PUTZ. 2008a. Beyond reduced-impact logging: Silvicultural treatments to increase growth rates of tropical trees. For. Ecol. Manage. 256: 1458–1467. PERES, C. A., J. BARLOW, AND W. F. LAURANCE. 2006. Detecting anthropogenic disturbance in tropical forest. Trends Ecol. Evol. 21: 227–229. PERLIN, J. 1991. A forest journey. Harvard University Press, Cambridge, Massachusetts. PERZ, S. G. 2007. Grand theory and context-specificity in the study of forest dynamics: Forest transition theory and other directions. Profess. Georgr. 59: 105–114. 19 PICKETT, S. T. A., AND V. T. PARKER. 1995. Avoiding the old pitfalls: Opportunities in a new discipline. Rest. Ecol. 2: 75–79. POSEY, D. A. 1984. A preliminary report on diversified management of tropical forest by the Kayapo Indians of the Brazilian Amazon. Adv. Econ. Bot. 1: 112–126. PUTZ, F. E., P. ZUIDEMA, M. A. PINARD, R. G. A. BOOT, J. A. SAYER, D. SHEIL, P. SIST, ELIAS, AND J. K. VANCLAY. 2008. Tropical forest management for carbon retention. PLOS Biology 6: 1368–1369. RACKHAM, O. 1998. Savanna in Europe. In K. J. Kirby and C. Watkins (Eds.). The ecological history of European forests, pp. 1–24. CAB International, Oxford, UK. REDFORD, K. H. 1992. The empty forest. BioScience 42: 412–422. RICHARDS, P. W. 1952. The tropical rain forest. Cambridge University Press, Cambridge, UK. ROBINSON, G. O. 1975. The forest service. Johns Hopkins Press, Baltimore, Maryland. ROBINSON, J. G., AND E. L. BENNETT. 2004. Having your wildlife and eating it too: An analysis of hunting sustainability across tropical ecosystems. Anim. Conser. 7: 397–408. ROOSEVELT, A. C. 1980. Prehistoric maize and manioc subsistence along the Amazon and Orinoco. Academic Press, New York, New York. RUDEL, T. K., D. BATES, AND R. MACHINGUIASHI. 2002. A tropical forest transition? Agricultural change, out-migration, and secondary forests in the Ecuadorian Amazon. Ann. Assoc. Am. Geogr. 92: 87–102. RUDEL, T. K., O. T. COOMES, E. MORAN, AND F. ACHARD. 2005. Forest transitions: Towards a global understanding of land use change. Global Environ. Change 15A: 23–31. SAHLINS, P. 1994. Forest rites: The war of the Demoiselles in nineteenth-century France. Harvard University Press, Cambridge, Massachusetts. SCHIMPER, A. F. W. 1903. Plant geography upon a physiological basis. (transl. W.R. Fisher, P. Groom, and I.B. Balfour). Oxford University Press, Oxford, UK. SCHOENE, D., W. KILLMANN, H. VON LUPKE, AND M. LOYCHEWILKIE. 2007. Definitional issues related to reducing emissions from deforestation in developing countries. Forests and Climate Change Working Paper No. 5, FAO, Rome, Italy. SHEPHERD, J. 1975. The forest killers. Weybright and Talley, New York, New York. SOUTHWORTH, J., H. NAGENDRA, AND L. CASSIDY. In press. Evaluating forest transition pathways in Asia: Case studies from Nepal, India, Thailand and Cambodia. Biotropica. STEEN, H. K. 1976. The U.S. Forest Service: A history. University of Washington Press, Seattle, Washington. STERN, N. 2006. The economics of climate change, the Stern review. Cambridge University Press, Cambridge, UK. TERBORGH, J., G. NUNEZ-ITURRI, N. C. A. PITMAN, F. H. CORNEJO VALVERDE, P. ALVAREZ, V. SWARNY, E. G. PRINGLE, AND C. E. T. PAINE. 2008. Tree recruitment in an empty forest. Ecology 89: 1757–1768. TRACEY, J. G. 1982. The vegetation of the humid tropical region of North Queensland. CSIRO, Melbourne, Australia. TSING, A. L. 2005. Friction: An ethnography of global connection. Princeton University Press, Princeton, New Jersey. TUCKER, C. M., J. C. RANDOLPH, T. EVANS, K. P. ANDERSSON, L. PERSHA, AND G. M. GREEN. 2008. An approach to assess relative degradation in dissimilar forests: toward a comparative assessment of institutional outcomes. Ecology and Society 13 (1): 4[online]: http.ecologyandsociety. org/vol13/iss1/art4/ UNFCCC. 2006. Background paper for the workshop on reducing emissions from deforestation in developing countries. UNFCCC, Rome, Italy. VERA, F. W. M. 2000. Grazing ecology and forest history. CAB International, Oxford, UK. VERCHOT, L. V., R. ZOMER, O. VAN STRAATEN, AND B. MUYS. 2007. Implications of country-level decisions on the specification of crown cover in the SPECIAL SECTION 20 Putz and Redford definition of forests for the land area eligible for afforestation and reforestation in the CDM. Climate Change 81: 415–430. WADSWORTH, F. H., AND J. C. ZWEEDE. 2006. Liberation: Acceptable production of tropical forest timber. For. Ecol. Manage. 209: 3–18. WALKER, A. 2005. Seeing farmers for the trees: Community forestry and the arborealisation of agriculture in Northern Thailand. Asia Pacific Viewpoint 45: 311–324. WALTER, H. 1971. Ecology of tropical and subtropical vegetation. (trans. D. Mueller-Dombois and J.H. Burnett), Van Nostrand Reinhold Company, New York, New York. WATKINS, C. 1998. A solemn and gloomy umbrage: Changing interpretations of the ancient oaks of Sherwood Forest. In C. Watkins (Ed.). European woods and forests: Studies in cultural history, pp. 93–113. CAB International, Oxford, UK. WEAVER, J. E., AND F. E. CLEMENTS. 1929. Plant ecology. McGraw-Hill Book Company, New York, New York. WEBSTER, N. 1983. Webster’s deluxe unabridged dictionary. Dorset and Baber, New York, New York. WESTOBY, J. 1989. Introduction to world forestry: People and their trees. Basil Blackwell, New York, New York. WILLIAMS, M. 2003. Deforesting the earth: From prehistory to global crisis. University of Chicago Press, Chicago, Illinois. YOUNG, C. R. 1979. The royal forests of medieval England. University of Pennsylvania Press, Philadelphia, Pennsylvania. ZOMER, R. J., A. TRABUCCO, L. V. VERCHOT, AND B. MUYS. 2008. Land area eligible for afforestation and reforestation within the Clean Development Mechanism: A global analysis of the impact of forest definition. Mitig. Adapt. Strat. Global Change 13: 219–239.
© Copyright 2026 Paperzz