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1
Commentary
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3
Nature conservation at the edge
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5
Jan Christian Habel1*, Mike Teucher2, Ronald K. Mulwa3, Wolfgang Haber4,
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Hilde Eggermont5,6, Luc Lens7
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School of Life Sciences Weihenstephan, Technische Universität München, D-85354 Freising,
Terrestrial Ecology Research Group, Department of Ecology and Ecosystem Management,
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Germany
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2
Department of Cartography, Trier University, D-54286 Trier, Germany
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3
Zoology Department, National Museums of Kenya, K-00100 Nairobi, Kenya
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Department of Ecology and Ecosystem Management, School of Life Sciences
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Weihenstephan, Technische Universität München, D-85354 Freising, Germany
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1000 Brussels, Belgium
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Limnology Unit, Department of Biology, Ghent University, B-9000 Ghent, Belgium
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Terrestrial Ecology Unit, Department of Biology, Ghent University, B-9000 Ghent, Belgium
Belgian Biodiversity Platform, OD Nature, Royal Belgian Institute of Natural Sciences, B-
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*Corresponding author:
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Jan Christian Habel, Terrestrial Ecology Research Group, Department of Ecology and
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Ecosystem Management, School of Life Sciences Weihenstephan, Technische Universität
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München, Hans-Carl-von-Carlowitz-Platz 2, D-85354 Freising, Germany
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E-Mail: [email protected]
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Key-words: Agro-ecological zone, biodiversity, cash crop, evidence-based conservation, food
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security, food crop, human population, nature reserve, prioritization
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ABSTRACT
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Currently, there is an increasing need for evidence-based strategies in nature conservation, for
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example when designing and establishing nature reserves. In this contribution, we critically
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assess the ecological relevance of recent nature conservation practices in Kenya (East Africa),
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a region of global biodiversity hotspots. More specifically, we overlay the distribution of
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species richness (here based on mammals, birds, amphibians and vascular plants) with the
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location of nature reserves, the Kenyan agro-ecological zones (areas representing diverging
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agricultural potentials), and with the spatial distribution of human population density. Our
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analyses indicate that the majority of protected areas are located in areas with comparatively
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low species richness, while areas with extraordinary high levels of species richness are not
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adequately covered by protected areas. Areas of high agricultural productivity (and with high
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human demographic pressure) are mainly reserved for high-yield agriculture; however, these
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regions are also characterised by high species richness. The majority of nature reserves are
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restricted to the semi-arid regions of Kenya, marginal for agricultural usage, but also with low
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levels of species richness. Based on this analysis, we prioritize areas for future protection.
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This single-country case illustrates that agricultural production in high-yield areas outweighs
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nature conservation goals, even in global biodiversity hotspot regions, and that priority setting
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may conflict with effective nature conservation.
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Introduction
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Recent studies critically examined the efficiency and relevance of nature conservation, which
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often focuses on the protection of large and charismatic species (rather than of species with
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high ecological relevance, or species groups like arthropods providing the mass of
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biodiversity, see Stork & Habel 2014), maintenance of specific successional stages of selected
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ecosystems (Rodrigues et al. 2006), or the conservation of man-made landscapes, in particular
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in Europe (Plieninger et al. 2006). In the meantime, other studies from scientists and
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practitioners plea for a revolution in nature conservation, towards more objectivity in
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conservation strategies with management based on ecological evidences rather than on
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political agendas (Pullin & Knight 2003, Sutherland et al. 2004, Svancara et al. 2005).
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Most of the established nature reserves in Sub-Saharan Africa are a legacy from the past
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colonial era (MacKenzie 1997, Lindsey et al. 2007). Examples are the vast savannahs in
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semiarid regions such as the Lowveld in Southern Africa or the Mara-Serengeti plains in East
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Africa. These nature reserves form the main body of wildlife tourism and nature conservation,
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and have high economic importance for many African countries (e.g. the Kenyan National
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Parks, with >2 billion visitors per year, KNBS 2014; 12.1% of the GDP and 9.2% of total
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employment (WTTC 2015)). However, most of these lowland protected areas are
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characterised by marginal agricultural value and low ecological productivity, and hold a
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comparatively small proportion of the total species richness too (Waide et al. 1999).
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In this commentary, we question the ecological relevance of many of these selected areas for
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nature conservation in Sub-Saharan African countries, and we illustrate our case with Kenya,
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one of the leading countries in African wildlife conservation and tourism. We therefore
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performed a country-wide assessment of (i) the distribution of species richness based on
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mammals, birds, amphibians and vascular plants (cross-taxon consensus percentage of species
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occurrence per 25x25 km grid cell), and of global biodiversity hotspots (according to
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Conservation International; Myers et al. 2000, Mittermeier et al. 2011); (ii) the location of
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nature conservation reserves (protected areas according to IUCN and UNEP-WCMC (2015)
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categories, including governmental and private conservation areas); (iii) the distribution of
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agro-ecological zones (AEZs) based on temperature, rainfall regimes and altitude; and (iv) the
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distribution of the human population using census data of the year 2009 (KNBS 2015). In a
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second step, we assessed potential spatial congruencies and discongruencies by creating a
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consensus map of species richness based on the four taxa studied and spatially overlapping
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this map with the current location of nature reserves (Fig. 1), AEZs, and human population
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data (Fig. 2).
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Centres of species richness beyond protected areas
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At present, Kenya holds 249 governmental and non-governmental (private conservancies)
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nature reserves that jointly cover about 8% of the country. However, the distribution of these
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nature reserves is geographically uneven. Likewise, species richness is unevenly distributed,
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with areas of high (endemic) species accumulation across the Eastern Afromontane region
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(e.g. Taita Hills, Chyulu Hills, Central Kenyan highlands including the Aberdares, Mau
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Escarpment or Mt. Kenya, as well as the mountain ranges in the north of Kenya) and the
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Coastal Forests (both regions classified as global biodiversity hotspots, Mittermeier et al.
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2011; see also Bennun and Njoroge 1999, Burgess et al. 2007) (Appendix S1). This spatial
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distribution of high species richness is congruent with former studies on amphibians and
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reptiles (Spawls et al. 2002, Lötters et al. 2007, Poynton et al. 2007, Measey et al. 2009),
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birds (Zimmermann et al. 1999), butterflies (Larsen 1991), and vascular plants (Lovett 1998,
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Burgess et al. 2005, Platts et al. 2010).
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Our intersect analyses indicate that areas with high levels of species richness only cover
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20.2% of the total area of Kenya - the highlands. But, o nly a very small proportion (14.1%)
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of protected land is located in these highland regions (FAO 2009), and only 56 of the 249
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nature reserves in Kenya (22.5%) overlap with the Eastern Afromontane and Coastal Forests
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biodiversity hotspots. Only 20% (1,795,730ha) of protected areas cover regions with
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extraordinary high species richness (>40% of the mean number of species over all taxonomic
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groups analysed here). In reverse, 80% of all nature reserves are located beyond regions of
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high levels of species richness. The top ten grid cells with highest levels of species richness
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can be found in the Western and Central part of Kenya (protected by Kakamega and Nandi
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forest, Aberdare forest reserve, Kikuyu Escarpment, Mt. Longonot, Moguga Forest, and Lake
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Niavasha). But even these areas are only partially covered by nature reserves (Appendix S2).
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Furthermore, most of nature reserves found at higher elevations are comparatively small
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(266.2±435.1km²) compared to the mean size of nature reserves in Kenya (387.2±1125.1km²).
113
This disparity between spatial distribution of species richness and the location and extent of
114
nature reserves seems to be a worldwide phenomenon, as indicated by Burgess and colleagues
115
(2005). Criteria used to define conservation areas are therefore questionable.
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Protected areas and agro-ecological zones
118
We used data from the Farm Management Handbook of Kenya (FMHB; Jaetzold et al. 2012)
119
to better understand the above-mentioned discrepancy between the distribution of species
120
richness and nature reserves. The FMHB provides a substantial long-term country-wide
121
survey of biotic and abiotic data, such as rainfall patterns, temperature, soil type, soil fertility
122
and census data on the human population density (Jaetzold et al. 2012). Based on a matrix of
123
a six-step altitudinal temperature gradient and a seven-step potential evapotranspiration (PET)
124
gradient, ranging from 0.1 PET to 1.25 PET, a total of 42 combinations of agro-ecological
6
125
zones (AEZ) are distinguished in Kenya. These AEZs range from high to low (i.e. a complete
126
lack of) agricultural productivity (Jaetzold et al. 2012). For our study, we further assigned
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these zones into four categories according to the PET-based humidity-aridity gradient, in
128
order to establish an altitudinal independent classification of agricultural productivity with
129
high potential (AEZ 0-2), medium potential (AEZ 3 and 4), low potential (AEZ 5) and very
130
low potential (AEZ 6 and 7). We spatially overlapped these AEZs with (i) areas conserved by
131
any nature protection status, and (ii) the distribution of the human population density.
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133
According to these FMHB data, 81.4% of the Kenyan land is semi-arid to arid, and thus of
134
marginal agricultural value (so-called `worthless land´). When overlapping these AEZs with
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areas that are protected to some degree, we found that most protected areas are restricted to
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land of low agricultural value (characterised by comparatively low precipitation and
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periodically sparsely occurring rainfalls). Vice versa, only 13.2% of protected areas are found
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within AEZs of high agricultural potential (AEZ 1 and 2), and only 8.5% within areas of
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medium agricultural value (AEZ 3 and AEZ 4). This picture is independent of the type of
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protection, i.e. governmental (e.g. National Park) or non-governmental (e.g. Game
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Conservancy). The spatial configuration is displayed in Figure 2. Further details on AEZ-
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nature reserve overlaps (distinguished between governmental and non-governmental) are
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given in Table 1.
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The spatial distribution and dominance of the AEZ with low agricultural potential underlines
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the economic impact of agro-industries in many African and other developing countries
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(Habel et al. 2015 with references therein). More specifically, Kenya´s economy highly
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depends on cash-crop production representing 19.4% of the GDP and 95.2% of total
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employment (alongside tourism, mining and manufacturing) (Kiteme et al. 2008; Worldbank
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2015, WTTC 2015). As a consequence, areas of high productivity (in Kenya mainly found in
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highland regions) are heavily exploited for food and cash-crop production (especially since
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the colonial era), while nature protection is restricted to regions with low (or no) agricultural
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importance.
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Biodiversity, nature conservation and human population pressure
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The semi-arid lowlands, holding many nature reserves, have been suffering from increasing
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human pressure and (over)exploitation of natural resources, like soils (KNBS 2015). The
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increase in human population was particularly high during the colonial period, when highly
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productive regions (the White-Highlands, Laikipia Plateau, Uasin Gishu Plateau; Jaetzold et
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al. 2006, 2011) were transformed into cash-crop monocultures (Habel et al. 2015) and many
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of the former local people had to move out from these highlands, and shifted to lowland areas
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(Kipkorir 1978, Thurston 1987). A first census on the Kenyan human population size
163
estimates about 2 million people at the beginning of the 20th century, and by the end of the
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colonial period in 1962 the human population had increased to 8.1 million people. Thereafter
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(i.e. past 30 years), the human population further increased with more than 250% - i.e. from
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16.26 million people in 1980 up to 40.9 in 2010 (Republic of Kenya 1964, KNBS 2015). This
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situation caused an increasing parcelling of land-plots, and a rising need for more land to
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produce enough food crops, with negative effects on ecosystem functions and services. Food
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crop yields per ha, however, stagnated (e.g. from 1980 to 2012, production increased with
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about 160% whereas yields per hectar increased by only 140%; FAOSTAT 2014).
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Subsequently, the land needed to produce the same amount of food increased. This resulted in
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conflicts between the production of cash-crops (agro-economy), food crops (subsistence
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agriculture), and nature conservation across Kenya (Habel et al. 2015). Furthermore, wildlife-
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conflicts arised especially along the borders of protected areas with, for example, illegal
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logging in the Taita Hills cloud forest and the Kakamega forest, illegal hunting in Arabuko
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Sokoke forest (Wildlifedirect 2009), and illegal pastoralism in vast areas of Tsavo and Mara
8
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National Parks (Okello & Kiringe 2004, Kiringe & Okello 2007, FAO 2009, Job & Paesler
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2013). Today, several protected areas are fenced (e.g. Aberdares, Nairobi, Nakuru, Marsabit
179
and Mt Kenya, Arabuko Sokoke National Park), not only to reduce conflicts between wildlife
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and humans, but also to prevent activities of local people inside these protected areas. This
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`gated conservation´ strategy might be the only viable solution, especially in densely
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populated areas. Yet, it prevents any participation by the local community and the long-term
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acceptance of people. as well as migration of wildlife among protected areas. The long-term
184
efficiency of such actions therefore remains highly questionable.
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Prioritizing areas for future conservation activity
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Our overlap analyses show that nature conservation strategies in Kenya mainly focus on areas
188
with rather low species richness, while areas of high ecological relevance are mostly typified
189
by high agricultural productivity, and thus often reserved for agricultural purposes.
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Accordingly, demographic pressure in such areas is exceptionally high. We found that some
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regions, such as the southern and south-western parts of Kenya as well as the coastal region,
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show extraordinary high levels of species richness, but are without any - or only under
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marginal - nature protection. This study hence underlines that the occurrence of the “big five”
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(African lion Panthera leo, African elephant Loxodonta africana, African buffalo Syncerus
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caffer, African leopard Panthera pardus pardus, and the African rhinoceros Diceros bicornis
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i.e. Ceratotherium simum) still seems to be the decisive factor when selecting nature reserves
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due to there importance for Kenya’s tourism, while the protection of prime biodiversity
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regions seems to be of lesser priority.
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Acknowledgement
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We are grateful to Ralph Jaetzold and Berthold Hornetz (Trier, Germany) for providing the
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valuable data-sets of the FMHB. We thank one anonymous referees for critical comments on
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a draft version of this contribution.
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1
Figure 1: Overlap of all Kenyan nature reserves (governmental and non-governmental) (white
2
lines) with species richness (consensus percentage value across four taxa in relation to the
3
total number of species known for Kenya), classified into five categories. Species richness
4
includes distribution data of the following taxonomic groups: mammals and amphibians (data
5
from the IUCN Red List of threatened species, digital distribution maps), birds (data from
6
BirdLife International and NatureServe 2015), and vascular plants (data from Kier et al.
7
2005). Data were trimmed to fit for Kenya using the clip function in ArcGis, and transformed
8
into a 25x25km grid.
9
10
15
1
Figure 2: Overlap of all 249 governmental and non-governmental protected areas (data from
2
IUCN and UNEP-WCMC 2015) (black shaded), the four categories of AEZs (according to
3
FMHB), and the distribution of the human population density (inhabitants per ha) (data from
4
KNBS 2015).
5
6
16
1
Table 1: Overlap between agro-ecological zones (divided into four categories, data obtained
2
from FMHB) and protected areas (governmental and non-governmental, distinguished).
3
Values are expressed as percentages.
Type of reserve
Governmental
Forest Reserve
Marine National Park
Marine National Reserve
National Park
National Reserve
National Sanctuary
Not Reported
Total (Gov.)[%]
Non-governmental
Community Conservancy
Community Nature Reserve
Community Wildlife Sanctuary
Group Ranch
Private Nature Reserve
Private Protected Area
Private Ranch
Wildlife Sanctuary
Total (Non-gov.) [%]
Total (both) [%]
AEZ
very low
AEZ
AEZ
low medium
AEZ
high
Total
[%]
0.93
38.58
17.35
59.86
1.89
2.15
3.36
0.09
7.49
5.85
0.04
0.03
1.11
3.52
0.19
0.01
10.75
15.11
2.46
0.12
17.69
23.78
0.04
0.03
44.30
24.35
0.28
0.01
64.17
5.23
75.06
0.58
0.08
0.08
0.06
0.89
0.18
82.15
67.88
2.59
8.25
0.06
0.11
0.50
1.48
0.95
0.14
14.07
10.45
0.19
3.51
0.01
0.01
0.06
3.78
8.48
13.19
8.01
86.82
0.65
0.20
0.58
1.54
1.90
0.32
35.83
100.00
4
17
1
Electronic Appendix Supplementary Material 1: Distribution of species richness of terrestrial
2
mammals, amphibians, birds and vascular plants in relation to the total number species known
3
for Kenya. Species richness grouped into 10% classes (to a maximum of 70%), and displayed
4
as 25x25km grid cells.
5
6
18
1
Electronic Appendix Supplementary Material 2: Location of the 10 grid cells with highest
2
species richness (over all four taxonomic groups assessed), displayed as grey squares,
3
intersected by existing nature reserves.
4
19