Abstract
Bio-cultural landscapes are characterized by anthropogenic pattern features, of which the measurement constitutes a key step in landscape analysis. Metrics and strategies for this measurement of anthropogenic patterns and their dynamics are discussed, considering the pattern/process paradigm, the patch-corridor-matrix model and the complementarity of landscape composition and configuration as conceptual benchmarks. Historically, noticeable anthropogenic effects are accepted to have appeared in landscapes after the invention of agriculture and further trends of landscape change could be linked to the development of agriculture. Through time, a sequence of landscape dynamics with three stages is expected, in which a natural landscape matrix is initially substituted by an agricultural one; urban patch types will later on dominate the matrix as a consequence of ongoing urbanization. The importance of the development of agriculture and its productivity for the evolution of settlements, villages and cities is emphasized. Anthropogenic change of landscapes confirms the status of geographical space as a limited resource.
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8.1 Bio-cultural Landscapes and Anthropogenic Patterns
More than 75 % of the Earth’s ice-free land shows evidence of alteration as a result of human residence and land use, with less than a quarter remaining as wildlands (Ellis and Ramankutty 2008). Globally most landscapes are blends of human activities with the expression of biodiversity, i.e. they are bio-cultural landscapes (Bridgewater and Arico 2002). This relationship between biological and cultural diversity has not been explored as biodiversity itself; this study of bio-cultural diversity involves a search for patterns across landscapes (Stepp et al. 2005). An intrinsic reciprocal relationship between culture and landscape structure exists: culture changes landscapes and culture is embodied by landscapes (Nassauer 1995).
In the current contribution, the cultural component of landscapes is generalized to the large-scale spatial footprint of Man’s actions, which refer to agriculture, urbanization, industrial development, road infrastructure or any other substitution or alteration of an original natural land cover by an anthropogenic type. This latter process is denoted as “anthropization” (Bogaert et al. 2011b); the modification of landscapes by human action leads to anthropogenic landscapes, in which man-made features dominate and the original natural patch types often are reduced to a scattered pattern.
A series of typical changes in landscape and biological characteristics during the conversion of natural lands to human-dominated landscapes has been reported (August et al. 2002). Hobbs and Hopkins (1990) in McIntyre and Hobbs (1999) expressed the range of human effects on landscapes in terms of the prevalent land use and using four levels: conservation of a more or less unmodified system, utilization of components of the system (e.g., forestry), replacement of the system by another type (e.g., agriculture), and complete destruction (e.g., urban development). Anthropogenic activities that require much space and which destroy or replace original land covers will consequently dominate human-driven landscape dynamics; they are considered exogenous disturbances (McIntyre and Hobbs 1999; Fischer and Lindenmayer 2007). This human impact on ecosystems and landscapes has lead to the recognition of 18 “anthropogenic biomes”, grouped in dense settlements, villages, croplands, rangelands and forested (Ellis and Ramankutty 2008).
Landscape ecology focuses on landscape pattern (Bogaert et al. 2011b; Bogaert and André 2013). Its central hypothesis is known as the pattern/process paradigm, which states that patterns and processes in landscapes are related in a way that landscape patterns condition those processes characterized by a spatial dimension, and that processes occurring in a landscape can modify landscape patterns (Turner 1989; Coulson et al. 1999; Noon and Dale 2002). The propagation of fire in a landscape as a function of vegetation and soil patterns (Diouf et al. 2012), biodiversity patterns as a function of landscape fragmentation (Barima et al. 2010a; Bogaert et al. 2011a), edge effects on soil parameters (Alongo et al. 2013), gap pattern dynamics in stressed vegetations (Van Peer et al. 2001), vegetation pattern change due to atmospheric deposits of heavy metals (Vranken et al. 2013), or periodic vegetation communities and the mechanisms behind their dynamics (Deblauwe et al. 2008, 2011, 2012; Diouf et al. 2010), can be cited as examples or closely related topics. This focus on spatial pattern distinguishes landscape ecology from general ecology (Fahrig 2005).
Consequently, many metrics have been developed and tested, also by the current authors (e.g., Salvador-Van Eysenrode et al. 1998; Bogaert et al. 1999b, 2000a, c, d, 2001b, 2002a, b). Analyses have shown that many metrics were correlated or mathematically related (Bogaert et al. 2002a; Bogaert and Hong 2004). It is recommended that those metrics are used for analysis which capture orthogonal pattern features (Bogaert and Mahamane 2005; Bogaert et al. 2011b). Many metrics have found applications outside landscape ecology (e.g., Bogaert et al. 2002c; Li et al. 2005; Hufkens et al. 2008), which illustrates the validity of the metrics involved and the aforementioned paradigm across spatial and temporal scales. This pattern-orientated identity of landscape ecology has created links towards other concepts such as fractal theory (e.g., Bogaert et al. 2000a; Imre and Bogaert 2004, 2006; Bamba et al. 2009; Bogaert et al. 2011b) or percolation theory (e.g., Bogaert and Impens 1998; Bogaert et al. 1999b, 2000b).
Landscape elements are generally classified as patches, corridors or matrix (Forman and Godron 1986; Urban et al. 1987; Forman 1995). Patches form the basic units of landscape pattern, and reflect homogeneous conditions significantly different from their surroundings. Patches representing a same land cover form a patch type or class. The definition of patches and patch types requires an application of the contrast concept, which corresponds to the magnitude of the difference between two patch types with regard to an ecologically significant characteristic (Forman 1995; Farina 2000b). Generally, morphological or structural characteristics are considered, such as vegetation type, density or height (Reino et al. 2009; Watling and Orrock 2010). A high contrast between adjacent land cover types generates edge effects, considered a main consequence of patch type fragmentation (Bogaert et al. 2011a); metrics have been developed by the current authors to quantify its impact (e.g., Bogaert et al. 1999a, 2001a, c, 2011a; Bogaert 2001; Salvador-Van Eysenrode et al. 2002; Barima et al. 2011; Vranken et al. 2011; Iyongo Waya Mongo et al. 2012, 2013).
Corridors can be considered a special type of patches, characterized by linear forms, and crucial for the connectivity of a patch type (Bogaert and Mahamane 2005). It should be noted that in most analyses, patch type connectedness is quantified instead of connectivity; the former concept refers to the physical links between landscape elements while the latter concept refers to the perception of connectedness by a particular species or group (Fig. 8.1) (Bogaert et al. 2000d). Therefore, the difference between patches and corridors is merely functional and often ignored in pattern analysis. In Fischer and Lindenmayer (2007), a third type is distinguished, “ecological connectivity” which refers to the connectedness of ecological processes across multiple scales, including trophic relationships, disturbance processes and hydro-ecological flows; its measurement remains however complicated.
The landscape matrix is formed by these patch types (generally one single type but a co-dominance of two or more types cannot be excluded) dominating the landscape by their extent (Bogaert and Mahamane 2005); in case of the absence of a dominant patch type, the landscape is often considered a mosaic.
Urban et al. (1987) stated that the primary influence of Man is to rescale patterns in space and time. This relationship between temporal and spatial patterns is a key concept in landscape ecology (Turner et al. 2001; Wiens 2009). Every process is characterized by a particular temporal and spatial scale or range which defines its frequency or duration, and its extent (August et al. 2002). In general, larger time steps are characteristic for processes concerning larger areas, and vice versa. For example, global temperature change increases slowly while smaller areas have already shown significant changes over shorter time periods (Bogaert et al. 2002c). This space-time relationship can be used to detect anthropogenic landscape dynamics, since the speed and extent of land cover change indicate the cause of the dynamics, anthropogenic causes leading to rapid land cover change on a large extent (August et al. 2002; Wiens 2009).
The attention of landscape ecology for large scale patterns is directly related to the spatial scale that corresponds to landscapes. Hierarchy theory (Allen and Starr 1982; Urban et al. 1987; Forman 1995; Burel and Baudry 2003; Bogaert and Mahamane 2005) states that the biosphere can be considered a sequence of scales reflecting a range of complexity or spatial levels, starting with the biosphere itself and going down to the elementary particles composing atoms. Different levels are distinguished among which the landscape, situated directly above the ecosystem level. Thus, landscapes are composed of ecosystems, a vision which corresponds to the definition put forward by Forman and Godron (1986) and which can be shortened as “landscapes are eco-complexes”; small-scale pattern features are ignored when they correspond to the sub-patch level. Landscape ecology research is consequently posed from a scale of a few meters to a 1,000 km across which most ecological processes are completed (Farina 2000a; Farina et al. 2005).
8.2 Measuring Anthropogenic Patterns
Landscape pattern itself is generally divided in two components: landscape composition and landscape configuration (Bogaert et al. 2011b) (Fig. 8.2). Composition refers to the number of patch types present in the landscape, their area and their definition. Landscape configuration is conditioned by landscape composition and refers to the spatial arrangement and geometry of the patch types (shapes, sizes, density and dispersion of patches). Its assessment is based on a multi-scalar approach, integrating pattern features at the patch, patch type and landscape level. Juxtaposition between patch types can also be considered as a component of landscape configuration. Patch dispersion assessment is often limited to the detection of aggregated, random or uniform patterns (Havyarimana et al. 2013; Kumba et al. 2013; Rakotondrasoa et al. 2013).
Patch definition is the first step of a configuration analysis; it is based upon technical aspects such as the type of pixel connectivity considered in raster based data (4-connectivity is generally applied) and the application (or not) of the minimum mapping unit technique (Bogaert and Hong 2004; Bamba et al. 2008; Bogaert et al. 2008). Patch orientation and spatial resolution also influence the final size and shape of the patches.
The definition of patch types directly affects their number and areas (Colson et al. 2009; Bastin et al. 2011) and consequently, landscape composition. Landscape composition change is preferably assessed by a transition matrix (e.g., Forman and Godron 1986; Dale et al. 2002; Bamba et al. 2008; Barima et al. 2009, 2010b; Bogaert et al. 2011a; Diallo et al. 2011), which has two entries in a diachronic analysis, one for each land cover map. It is composed of three groups of values. Firstly, the row and column totals refer to the patch type areas for the first and second map, respectively. These data can be used for landscape matrix identification or for composition analysis by means of heterogeneity metrics, such as the Simpson or Shannon indices. Secondly, the central part of the transition matrix should be observed. Its values reflect transitions from the patch types on the rows to the patch types on the columns. This core part can be split up in two groups: the values on the diagonal, reflecting those areas which did not go through a change of their land cover, and the values outside the diagonal, representing land cover change. The higher the values on the diagonal relatively to those outside from it, the less dynamic a landscape was in the time period considered. To deal with a new patch type (i.e. a patch type not present on the first land cover map but appearing on the second map), a row should be inserted which contains only zero values. Patch types disappearing from the landscape will be characterized by the overall presence of zero values in their columns.
The interpretation of the transition matrix can be visualized by a scheme in which arrows indicate the areal exchanges between patch types. Metrics based on the transition matrix could be suggested. The ratio of the sum of the values outside the diagonal to the value on the diagonal could be used to express the dynamics of an individual patch type. Row and column values will enable distinct interpretation. The row values will reflect the tendency of the patch type to lose area to other types; the column values will reflect the tendency of the patch type to increase its extent through land cover change of other patch types. Analogously, the ratio of the sum of the values on the diagonal to the sum of the values outside the diagonal will reflect overall landscape dynamics; in case of maximum dynamics (every areal unit of the landscape is converted into another patch type), this ratio will equal zero; in case of a perfectly static landscape, the ratio will equal infinity.
To detect anthropogenic effects, the nature of the patch types should be taken into account. Exchanges in favor of anthropogenic classes such as urban zones or agricultural patch types will reflect a decrease in the degree of naturalness of the landscape. An application of the landscape disturbance index (O’Neill et al. 1988; August et al. 2002; Barima et al. 2011; Bogaert et al. 2011b; Mama et al. 2013) seems useful in this context. It can be used to verify the hypothesis which relates increasing landscape entropy, i.e. spatial compositional heterogeneity, to higher levels of anthropogenic impact (Bogaert et al. 2005). Figure 8.3 shows that maximum entropy is to be observed at intermediate levels of anthropogenic influence. The aforementioned trends observed by Bogaert et al. (2005) seem to correspond to the upward parts of the curves. The bell-shaped trends in Fig. 8.3 are not unexpected: the extremities of the curves correspond to landscapes with high dominance, hence low heterogeneity; in between, equilibrium of anthropogenic and natural types is expected, characterized by higher index values for heterogeneity and evenness. This has noteworthy perspectives since entropy is considered a driver of biodiversity (Fahrig et al. 2011).
The transition matrix can be used to simulate future landscape evolution (Urban and Wallin 2002; Barima et al. 2010b, 2011; Vranken et al. 2011; Toyi et al. 2013a). To decouple simulations from the time periods characterizing the transition matrix, annual probabilities of landscape change are to be determined. This operation is still subject to debate. The algorithm proposed by Urban and Wallin (2002) could not always be validated (data not shown). The determination of these annual probabilities seems more difficult than expected, and requires a profound mathematical analysis, as shown by Takada et al. (2010).
Patch shape analysis represents a central activity in pattern assessment. Two main analysis types can be distinguished. Firstly, patch shape can be compared to a reference shape, generally an isodiametric one such as a disk or square (Patton 1975; Bogaert et al. 2000c; Bogaert 2001). This analysis is useful when estimating edge effects, which are proportionally larger for elongated or complex shapes than for isodiametric ones of equal area (Forman and Godron 1986; Toyi et al. 2013b). The difference between both shapes can then be expressed by means of a perimeter-to-area ratio, obligatory dimensionless to avoid size effects (Fig. 8.4). Perimeter-to-area ratios are generally based on the isoperimetric principle, which states that of all shapes with an equal perimeter, the disk is characterized by the largest area (Fig. 8.5); the principle could also be interpreted otherwise: of all shapes with an equal area, the disk is characterized by the shortest perimeter. For raster based data, the reference perimeter does not correspond to a circular shape but is a function of the number of pixels composing the patch (Bogaert et al. 2000c; Bogaert and Hong 2004).
The second type of shape analysis consists of the determination of the fractal dimension. Since it cannot be determined for a single patch (i.e. when multi-scalar information is not available), a regression technique is applied to estimate it for a group of patches with similar geometry (Krummel et al. 1987; Imre and Bogaert 2004; Bamba et al. 2009, 2010; Bogaert et al. 2011b; Colson et al. 2011; Diallo et al. 2011). The statistical regression parameters can consequently be interpreted to validate this hypothesis; to guide the analyst in its selection, a common origin of the patches, i.e. a common shape-forming process, could be suggested. In case of shape regularity, which indicates anthropogenic effects, the fractal dimension will tend towards one; for increasing patch complexity, associated with natural patch forming processes, fractal dimension will be significantly higher, with two as its upper bound.
A relationship has been shown between patch size and fractal dimension (Krummel et al. 1987); larger patches are expected to be characterized by a larger fractal dimension since their shapes are determined by natural patterns, such as geomorphologic discontinuities; small patches are often anthropogenic and even when they are natural, their shape is usually determined by adjacent anthropogenic patches. Nevertheless, it should be noted that aggregation of anthropogenic patches can generate complex patch geometries which could be confounded with natural landscape elements (Fig. 8.6).
The dynamics of a patch type can be characterized by the identification of the corresponding transformation process (Forman 1995; Jaeger 2000; Bogaert et al. 2004, 2008; Koffi et al. 2007; Vranken et al. 2011). As for a transition matrix, two land cover maps are needed in a diachronic analysis; the analysis is done per patch type. The current technique has the advantage that it is based on basic pattern information (number of patches, patch type area, patch type perimeter) and that it is applicable to patch types with decreasing or increasing area, hence for natural and anthropogenic types, the latter generally characterized by an increase in their extent in time when anthropogenic effects become more dominant. A second advantage is the availability of a decision tree model which guides the analyst directly to the spatial transformation process for the patch type considered; in order to determine the transformation process, the model uses comparisons of the number of patches, patch type area and patch type perimeter before and after transformation of the type (e.g., Bogaert et al. 2004, 2008; Barima et al. 2009; Diallo et al. 2011).
The idea behind the transformation processes is that land cover dynamics can be represented by series of well-defined pattern change types. In a time series analysis, a process will be determined for each pair of land cover maps. Ten spatial transformation processes have been defined: aggregation, attrition, creation, deformation, dissection, enlargement, fragmentation, perforation, shift and shrinkage. In case of anthropogenic landscape dynamics, natural patch types will be characterized by attrition, deformation, dissection, fragmentation, perforation and/or shrinkage; patch types reflecting anthropogenic activities will show aggregation, creation, deformation, enlargement and/or shift (Fig. 8.7) (Bogaert et al. 2011b).
According to Forman (1995) and Bogaert et al. (2004), the aforementioned processes often show well defined sequences: fragmentation is generally preceded by dissection and/or perforation, and followed by shrinkage and attrition; creation is often followed by enlargement which could in its turn lead to aggregation. However, other sequences should not be excluded (Fig. 8.7), since the temporal resolution of the data influences the determination of the processes and long time periods can hide a series of processes (Bogaert et al. 2004).
The decision tree model enables a distinction between fragmentation and dissection, since the ratio between the patch type area after transformation to the area before transformation is used as an indicator of the impact of the transformation; low values of the ratio are interpreted as fragmentation, while small changes of patch type area suggest landscape dissection (Bogaert et al. 2004; Barima et al. 2009; Diallo et al. 2011). In Forman (1995), no pattern difference was made between both processes. Presumably less significant changes of the patch type pattern, although often easily detectable when expressed as relative changes, could be countered by a double analysis: one considering the change as significant followed by one considering both values as equal.
8.3 Historical Perspective on Anthropogenic Effects in Landscapes
Anthropogenic effects refer to those land use and land cover dynamics which are caused by human activities. Since Man replaces natural land covers by anthropogenic ones, and since this substitution is not a random one, landscape pattern can be used to detect anthropogenic influence. Historically, noticeable anthropogenic effects are accepted to be associated with the start of agriculture (Fig. 8.8). No other activity has transformed humanity, and the Earth, as much as agriculture (Tilman 1998). In ecological terms, agriculture represents a symbiotic relationship between humans and domesticated plants and animals (Cox and Atkins 1979). It is evident that also earlier in time, i.e. before the invention of agriculture, anthropogenic effects should have occurred; however, due to the low population density, the local (or even sub-patch) character of the land cover changes and the non-sedentary character of the populations involved, they can be accepted of little or no significance. Before the invention of agriculture, it is supposed that Man lived in equilibrium with its environment and that all landscapes were natural landscapes.
Three ages are generally distinguished to subdivide the Holocene: the Paleolithic pre-agricultural era, which ended about 10,000 years BP, the agricultural era, between 10,000 years BP and the industrial revolution (~1800), and the agro-industrial era, since the industrial revolution (Cox and Atkins 1979; Smith 1989; Gupta 2004; Pinhasi et al. 2005; Sheaffer and Moncada 2009; Balaresque et al. 2010). Landscape-scale dynamics have occurred since man has become sedentary. This change of life style is accepted to have been directly related to the invention of agriculture in the Neolithic era. Early hominids were hunters and gatherers who relied on naturally occurring vegetation, fruits, nuts, carrion and game for subsistence (Gupta 2004; Sheaffer and Moncada 2009). Hunters and gatherers did not establish permanent settlements such as villages. They moved their camps in response to changes in the season and climate (Gupta 2004).
Among the most significant examples of human impact on the evolution of ecological niches come from domestication of animals and plants; domestication refers to the process of reciprocation, by which animal and plant species come to depend on humans for survival, while providing humans with numerous benefits in turn (Cox and Atkins 1979; Gupta 2004). The process of domestication has been markedly important for spatial expansion and population increase of humans during the Holocene (Soja 2003; Gupta 2004; Sheaffer and Moncada 2009). It is however noteworthy that this link between agricultural development and population growth is still subject to debate (Childe 1950; Kohl and Wright 1977; Armelagos et al. 1991). Domesticated species were of prime importance for agriculture: without agriculture, the complex, technically innovative societies and large human populations that exist today could not have evolved (Gupta 2004). Husbandry is consequently defined as the cultivation of domesticated plants and animals for use by human societies, as many domesticated plants and animals would not survive without human intervention (Gupta 2004). As for grain crops, the main selection criteria involved, next to increased plant yield, also increased seed size, non shattering seed, naked seed and reduced seed toxins (Sheaffer and Moncada 2009).
Agriculture allowed and even forced people to become sedentary, which can be defined as living for a prolonged period in one place, as establishing permanent villages and towns and as developing classified societies that included dedicated social or professional segments such as farmers, artisans, soldiers, religious leaders, teachers and governors (Gupta 2004). The shift from the nomadic life style of the hunters and gatherers to the sedentary one of the early farmers was suggested to have been a consequence of the larger amount of energy required for hunting and gathering than for agricultural practices to obtain the same calories of food energy (MacDonald 2003; in Gupta 2004), together with the intrinsic dynamics of human populations and more favorable climates leading to the exuberance of vegetation and diversification of the plant communities (Gupta 2004; Sheaffer and Moncada 2009).
It is appealing to detail these links between the start of husbandry, the founding of settlements, the development of villages, and the origin of cities. Increasing agricultural productivity is suggested as a key concept in this sequence. While agricultural production itself refers to the total quantity of biomass produced, the productivity concept expresses this quantity as a function of the production factors used (e.g., Van Zanden 1991). These factors can be numerous and heterogeneous, such as the time between the preparation of the land and the final yield, the number of farmers involved in production, the production surface used, energy inputs, or the quantities and types of fertilizers used. The nomadic lifestyle of Man before the development of agriculture and its dependence on natural rhythms and production had taught Man to observe and understand its environment. Through this necessity to adapt his life style to nature, Man acquired knowledge on the production of biomass in nature (Braidwood 1979; Sheaffer and Moncada 2009). Later on, agricultural productivity was increased, e.g. by use of energy provided by domesticated animals (Demangeon 1933; Childe 1950; Davis 1955; Kohl and Wright 1977; Smith 2009). This enabled individuals to leave the agricultural sector. Through this tendency, the initial agricultural settlements, which were still dominated by farmers and their families, were converted into (non-agricultural) villages, and later on, into urbanized zones. Between 6000 and 4000 B.C., certain innovations (such as the ox-drawn plow) facilitated, when taken together, a more intensive and more productive use of the Neolithic elements themselves; the rise of cities and towns required in addition to highly agricultural conditions, a form of social organization in which certain strata could appropriate part of the produce grown by the cultivators (Davis 1955).
One can agree with the dominant view that the diverse technological innovations constituting the Neolithic culture were necessary to the existence of settled communities (Davis 1955). Surprisingly, Soja (2003) states that no agricultural surplus was necessary for the development of cities, but that cities were necessary for the production of an agricultural surplus, at least in certain regions in the world. This hypothesis is denoted a persistent error in the non archeological literature: archeological records show quite clearly and consistently throughout the world that the Neolithic revolution (agriculture) occurred first, and only afterwards did the first cities emerge (Smith 2009).
It should be noted that land change to build cities and to support the demands of urban populations itself drives other types of environmental change: urban dwellers depend on the productive and assimilative capacities of ecosystems well beyond their city boundaries (ecological footprint concept), to provide the flows of energy, material goods and nonmaterial services that sustain human well-being and quality of life (Grimm et al. 2008; Vranken et al. 2011; Seto et al. 2012).
Agriculture also evolved throughout history. A tendency towards uniformity (of production systems and crops) on large scales has been observed (Ramade 2005), stimulated, amongst others, by the green revolution (Evanson and Gollin 2003), the sustainability and socioeconomic impacts of which have been criticized. New technologies have been applied, and high levels of energy input have become characteristic for production. The use of energy in multiple farming systems and for different crops has been debated (Cox and Atkins 1979; Cleveland 1995; Ramade 2005; Gliessman 2006; Pimentel and Pimentel 2008; Pimentel et al. 2008; Pimentel 2009; Sheaffer and Moncada 2009); larger energy inputs are not always coupled to higher energy efficiency. Moreover, a shift towards the production of feed and biofuels instead of food has been observed, despite their less favorable energy balance and environmental issues (Pimentel 2003; Pimentel and Patzek 2005; Gliessman 2006; Groom et al. 2008; Pimentel et al. 2009). Growing crops for biofuel not only ignores the need to reduce natural resource consumption, but exacerbates the problem of malnourishment worldwide by turning food grain into biofuel (Pimentel et al. 2009): this raises major ethical and moral issues (Pimentel 2003; Pimentel and Patzek 2005). The aforementioned trends, combined with the increasing demographic pressure, will have profound impacts on landscapes, since larger areas will be required to produce biomass to directly feed humans, to grow livestock, and to provide alternatives for fossil fuels. This potential spatial impact of biofuel production is discussed in Groom et al. (2008).
8.4 Agriculture and Urbanization: Matrix Competitors
Agricultural development from a local, low productive activity to an extensive, high yielding production process based on high energy inputs, has put his footprint on societies and landscapes. Through technical developments and concomitant fossil fuel consumption, one farmer has nowadays become able to produce more per unit area and on larger extents than ever before. Therefore, it can be accepted that agricultural land uses became dominant in landscapes through time and have replaced the original natural patch types, such as forests, by anthropogenic ones, such as fields, fallow lands, pasture lands or agricultural buildings. This tendency, often detected as deforestation, has been frequently observed (Lepers et al. 2005). This increase of patch types related to farming consequently decreased the cumulative area of natural areas; often only non fertile areas or difficultly accessible zones such as mountains or swamps were not converted into farmland. Land accessibility is often cited as the main cause of landscape change, next to their intrinsic properties (August et al. 2002). The landscape matrix, which has been dominated exclusively by natural patch types before the arrival of agriculture, was consequently systematically replaced by an anthropogenic, agricultural matrix (Figs 8.9 and 8.10). The area increase of the anthropogenic type(s) was mainly caused by patch creation, enlargement and aggregation. The decreasing overall area for the natural patch types was the consequence of perforation, dissection, fragmentation, shrinkage and attrition.
Not only total patch type area, but also the number of patches per type was influenced by this substitution (Fig. 8.11). Initially, both types, natural and anthropogenic, were characterized by an increase in their number of landscape elements. This increase could have been expected to be faster for the natural than for the anthropogenic types, since anthropogenic activities, especially farming, are considered to have been more efficient when aggregated in space: short distances between farmlands were preferred and adjacent lands even more. This increase in the number of patches slowed down when patches started aggregating (for anthropogenic types) or disappearing (for natural types). When the substitution had continued, finally both types would have been characterized by a low(er) number of patches, and the final frequencies of patches could then be described using the typology of Forman and Godron (1986) categorizing them in disturbance patches, remnant patches, introduced patches and environmental resource patches, according to their origin or cause of existence (Fig. 8.12).
This substitution of a natural matrix (of which the land cover types were mainly determined by the abiotic context, such as the climate or geomorphology) by an agricultural one could have been repeated later on, but this time when an urban matrix was replacing the formerly dominant agricultural one. Urbanization is namely expected to be dominant in contemporary landscapes, with a dominant urban world population projected for the middle of the twenty-first century (Grimm et al. 2008; Montgomery 2008); urban land cover could even increase by >1 million km2 by 2030, nearly tripling the global urban land area circa 2000 (Seto et al. 2012). For centuries, cities were compact with high population densities, with limited physical extents; this trend has been reversed over the last 30 years with urban areas that are nowadays expanding on average twice as fast than their populations (Seto et al. 2012). For the United States, a >30 % of increase of the amount of land devoted to urban and built-up uses between 1982 and 1997 was noted (Alig et al. 2004).
Two major pathways of urban impacts on land cover are to be considered. In the developed world, large-scale urban agglomerations and extended peri-urban settlements fragment the landscapes of such large areas that various ecosystem processes are threatened; however, ecosystem fragmentation in peri-urban regions may be offset by urban-led demands for conservation and recreational land uses; on the other hand, in less developed countries, urbanization seems to outbid all other uses for land adjacent to the city, including prime croplands (Lambin et al. 2001). Urban zones are characterized by rapid enlargement and the management of peri-urban zones, where rural and urban areas meet and conflict, announces itself as a key issue for landscape ecology in the near future, although an unambiguous functional and morphological definition and identification of peri-urban zones remains subject to debate (Fig. 8.13) (Forman 2008; André et al. 2012). These peri-urban environments are the glue that link core cities in extended urbanized regions (Grimm et al. 2008): the “edge” of the city expands into the surrounding rural landscape, including changes in soils, built structures, markets, and informal human settlements, all of which exert pressure on fringe ecosystems.
Thus, according to the aforementioned landscape dynamics model, which can be denoted as the “nature-agriculture-urban model”, natural landscapes are replaced by anthropogenic ones, initially dominated by agriculture, later on by land covers reflecting urban development. It should be noted, however, that there are different trajectories of land cover change in different parts of the world (e.g., decrease of cropland in temperate areas and increase in the tropics) (Lepers et al. 2005). This observation confirms the aforementioned model with tropical countries still expanding their agricultural matrix while in temperate zones the urbanization has already taken over, although a co-dominance of both agriculture and urbanization should not be excluded. Agricultural development and urbanization are not synchronized between developed and developing countries but since both hemispheres seem to follow the same model, the outcome of both evolutions is predictable. In Forman and Godron (1986) a similar, five-step anthropization gradient was presented, with natural, managed, cultivated, suburban and urban landscapes.
8.5 Concluding Commentary: Space Is a Limited Resource
The concept of limited (or not renewable) resources refers to those elements that can be extracted or consumed but for which the available quantity is considered well-defined. When a fraction of the resource is used, the remaining quantity consequently declines. Sometimes, this consumed quantity can be restored after a long period, but the delay is often too long to consider the resource as renewable. This concept of resource limitation can also be applied in landscape ecology. Landscapes are composed of different types of land cover which each occupy a fraction of a geographical space. This geographical space is limited, i.e. it corresponds to a well-defined extent. Consequently, space could and should be considered as a limited resource: the use of space by one land cover type reduces the remaining space available to other types.
This recognition of space as a limited resource underlines the importance of landscape ecology in preserving sufficient space with an optimal configuration to enable a coexistence of the development of anthropogenic activities with the preservation of ecosystem services (Costanza et al. 1997; Pimentel et al. 1997), even in an urban context (Bolund and Hunhammar 1999; Tratalos et al. 2007). For the foreseeable future, the fate of terrestrial ecosystems and the species they support will be intertwined with human systems: most of “nature” is nowadays embedded within anthropogenic mosaics of land use and land cover; while climate and geology have shaped ecosystems and evolution in the past, human forces may now outweigh these across most of Earth’s land surface today (Ellis and Ramankutty 2008).
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Isabelle Vranken is a research assistant at the FNRS, Belgium.
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Bogaert, J., Vranken, I., André, M. (2014). Anthropogenic Effects in Landscapes: Historical Context and Spatial Pattern. In: Hong, SK., Bogaert, J., Min, Q. (eds) Biocultural Landscapes. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-8941-7_8
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