Hostname: page-component-7c8c6479df-94d59 Total loading time: 0 Render date: 2024-03-28T12:19:09.628Z Has data issue: false hasContentIssue false

Population status of the Bornean orang-utan Pongo pygmaeus in a vanishing forest in Indonesia: the former Mega Rice Project

Published online by Cambridge University Press:  27 August 2014

Megan E. Cattau*
Affiliation:
Nicholas School of the Environment, Duke University, 450 Research Drive, Durham, NC 27708, USA.
Simon Husson
Affiliation:
Orangutan Tropical Peatland Project, Center for International Cooperation in the Sustainable Management of Tropical Peatlands, University of Palangka Raya, Central Kalimantan, Indonesia
Susan M. Cheyne
Affiliation:
Orangutan Tropical Peatland Project, Center for International Cooperation in the Sustainable Management of Tropical Peatlands, University of Palangka Raya, Central Kalimantan, Indonesia
*
(Corresponding author) E-mail mec2201@columbia.edu
Rights & Permissions [Opens in a new window]

Abstract

As peat-swamp forests in Borneo become progressively more fragmented, the species that inhabit them are increasingly threatened, notably the Endangered Bornean orang-utan Pongo pygmaeus. The area of a failed agricultural project known as the Mega Rice Project in Central Kalimantan, Indonesia, is composed of fragments of peat-swamp forest that are reported to contain orang-utans, although no comprehensive survey has previously been conducted. In a portion of this area we identified remaining forest fragments, using satellite imagery, and surveyed line transects for orang-utan sleeping nests to determine the density, abundance and distribution of the species. The total area of peat-swamp forest in the study area is 76,755 ha, 59,948 ha of which comprises patches at least as large as the home range of a female orang-utan (250 ha). We estimate a mean population density of 2.48 ± SE 0.32 individuals km−2 and a population of 1,700 ± SE 220 or 1,507 ± SE 195 individuals, based on a 25 and 250 ha minimum patch size threshold, respectively. This is c. 40–45% of the original population, and the fragmented population is unlikely to be viable in terms of long-term demographic and genetic stability. To ensure persistence of this population of orang-utans, direct conservation action to connect forest fragments and prevent further loss of peat-swamp forest will be required, including re-establishing the hydrological regime, reforesting barren areas and fighting fires.

Type
Papers
Copyright
Copyright © Fauna & Flora International 2014 

Introduction

In their natural condition, lowland peat-swamp forests in South-east Asia provide invaluable ecosystem services at local and global scales. They prevent flooding, resist large-scale fires and sequester and store carbon (Page & Rieley, Reference Page and Rieley1998; Page et al., Reference Page, Siegert, Rieley, Boehm, Jaya and Limin2002, Reference Page, Rieley, Wüst, Martini, Martínez Cortizas and Chesworth2006; Hooijer et al., Reference Hooijer, Silvius, Wösten and Page2006; Yule, Reference Yule2010). They are also rich in endemic, rare and threatened flora and fauna (Ng et al., Reference Ng, Tay and Lim1994; Yule, Reference Yule2010). However, peatland areas all over South-east Asia, including in Kalimantan, Indonesia, are being degraded and fragmented, in part as a result of the development of oil palm plantations, other forms of agriculture, logging and the secondary effects of these disturbances, including drainage, peat subsidence and fire (Barr, Reference Barr, Colfer and Resosudarmo2002; Hooijer et al., Reference Hooijer, Silvius, Wösten and Page2006; Koh et al., Reference Koh, Miettinen, Liew and Ghazoul2011). By 2006 c. 45% of South-east Asia's 27 million ha of peat forest had been deforested (Hooijer et al., Reference Hooijer, Silvius, Wösten and Page2006) and projections of deforestation under a business-as-usual scenario indicate that just under half of the peat-swamp forest in Central Kalimantan may be lost by 2020 (Fuller et al., Reference Fuller, Hardiono and Meijaard2011).

As the forests of South-east Asia become more sparse, species that depend on these areas for habitat or breeding are increasingly threatened (Sodhi et al., Reference Sodhi, Koh, Brook and Ng2004). Of particular note is the Bornean orang-utan Pongo pygmaeus because some of the highest densities of this species are found in lowland peat-swamp forest (Husson et al., Reference Husson, Wich., Marshall, Dennis, Ancrenaz, Brassey, Wich, Utami Atmoko, Mitra Setia and van Schaik2009). The Bornean orang-utan is categorized as Endangered on the IUCN Red List (Ancrenaz et al., Reference Ancrenaz, Marshall, Goossens, van Schaik, Sugardjito, Gumal and Wich2008), with a decreasing population trend attributed primarily to forest loss (Singleton et al., Reference Singleton, Wich, Husson, Stephens, Utami-Atmoro and Leighton2004; Ancrenaz et al., Reference Ancrenaz, Marshall, Goossens, van Schaik, Sugardjito, Gumal and Wich2008). Some researchers predict that the extinction of the orang-utan is imminent if current trends of forest loss continue (Rijksen & Meijaard, Reference Rijksen and Meijaard1999; Williams, Reference Williams2007; but see Meijaard & Wich, Reference Meijaard and Wich2007).

Effective conservation efforts for these great apes will require accurate baseline information on their density and distribution. This information will be particularly important in unprotected areas, which are home to the majority of orang-utans (Singleton et al., Reference Singleton, Wich, Husson, Stephens, Utami-Atmoro and Leighton2004; Wich et al., Reference Wich, Gaveau, Abram, Ancrenaz, Baccini and Brend2012) and which remain vulnerable to conversion for commercial purposes. We present the first spatially explicit, landscape-scale analysis that aims to describe the status of the population of southern Bornean orang-utans P. pygmaeus wurmbii that inhabit an unprotected area known as Block C of the former Mega Rice Project, Central Kalimantan, Indonesia. Specifically, our objectives are (1) to identify the remaining forest patches in Block C that contain orang-utans, and quantify the total area of habitat remaining, and (2) to estimate the density and size of viable populations of orang-utans in these patches.

Study area

The Mega Rice Project in Central Kalimantan, Indonesia, is a failed agricultural project that was initiated in 1995 (Presidential Decree RI/82-26, 1995). Over 1 million ha of lowland peat-swamp forest, of a total of 6.8 million ha in Kalimantan, were targeted for conversion into rice paddies (Boehm & Siegert, Reference Boehm and Siegert1999; Sabiham, Reference Sabiham, Furukawa, Nishibuchi, Kono and Kaida2004). Drainage and irrigation canals were constructed and forest was cleared. However, the project was abandoned because the soil proved to be too acidic for rice cultivation and the canals had drained the peat (Aldhous, Reference Aldhous2004).

Our study area is Block C of the Mega Rice Project, which comprises five blocks in total (Fig. 1). Drainage canals were built throughout Block C but the forest was never cleared. Nevertheless, nearly 70% of the original peat-swamp forest in Block C had been lost as of 2000 (Boehm & Siegert, Reference Boehm and Siegert2001), primarily as a result of fires caused by a combination of drought and drainage by canals during 1997–1998. Further forest loss was recorded during the dry seasons of 2002, 2004, 2006 and 2009. Block C remains designated for conversion to agriculture, and oil palm development has begun in the far south although the majority of Block C is protected under a temporary moratorium on logging and conversion. All of the fragmented forest patches in Block C are reported to contain orang-utans, but prior to this study no comprehensive census of the area had been conducted.

Fig. 1 Block C of the former Mega Rice Project in Central Kalimantan, Indonesia, including locations of orang-utan Pongo pygmaeus nests along survey transects.

Methods

Land cover analysis and habitat identification

A land cover assessment of the study area was conducted using satellite data (Landsat 7 ETM+ data acquired 19 May 2008, the closest date prior to the study period for which relatively cloud-free data are available). The data were radiometrically and atmospherically corrected and we completed a supervised classification, using a maximum-likelihood decision rule, to categorize the data for Block C into the following land cover/land use categories: mature forest, degraded or secondary forest, grassland/shrubland, sparsely vegetated, barren or recently burned, cloud, cloud shadow, and water/inundated. Training sites for spectral signatures were based on our on-the-ground knowledge of the study area and global positioning system points that we collected in the field for each land cover/land use category (i.e. ground-truthing points). Focal statistics were used to reassign values to the pixels with no data or classified as cloud and cloud shadow. Although agricultural areas were difficult to distinguish from other categories because of their high spectral variability, the visible fine-scale irrigation canals running throughout made it possible to hand-digitize the agricultural areas. We used an error matrix to conduct an accuracy assessment using the ground-truthing points that were withheld from model development. Overall classification accuracy was > 85%. Irrigation canals (referenced shapefiles provided by Agata Hoscilo of Leicester University, UK) were incorporated into this classified image, using ArcGIS v. 9.3 (ESRI, Redlands, USA). We distinguished peat-swamp forest from other forest, including freshwater swamp, mangrove and heath forests, based on our on-the-ground knowledge and ground-truthing points. To identify patches of suitable orang-utan habitat, we retained only the mature and secondary or degraded peat-swamp forest classes and excluded patches < 25 ha, which are unlikely to provide habitat for orang-utans. We chose a 250 ha minimum patch size threshold, at the lower end of the best estimate of minimum home range size of female P. pygmaeus wurmbii in Sabangau (Singleton et al., Reference Singleton, Knott, Morrogh-Bernard, Wich, van Schaik, Wich, Atmoko, Setia and van Schaik2009), to quantify remaining habitat that is likely to support orang-utans in the long term. Although it is possible that forest fragments < 250 ha contain resident orang-utans, fragments are isolated by burnt and deforested land, thus impeding movement between fragments and reducing the long-term viability of these fragments for orang-utans.

Density and population size estimation

Line-transect distance sampling (Buckland et al., Reference Buckland, Anderson, Burnham and Laake1993, Reference Buckland, Anderson, Burnham, Laake, Borchers and Thomas2001) for sleeping nests, a standard method for calculating ape abundance (Kuhl et al., Reference Kuhl, Maisels, Ancrenaz and Williamson2008), was conducted during June–July 2009 as part of a multi-disciplinary research project run jointly by the Orangutan Tropical Peatland Project and the Center for International Cooperation in the Sustainable Management of Tropical Peatlands. Line transects were hand-cut systematically, with random starting points, through all accessible forested patches in Block C (Fig. 1). We did not survey patches that were physically inaccessible or that the property owner did not give us permission to access. A total of 27 transects (with a total length of 26.3 km) were surveyed. Observers walked slowly along the transects, looking in all directions for orang-utan sleeping nests. For each nest sighted the distance along the transect and the perpendicular distance from the nest to the transect were measured.

We used DISTANCE v. 6.0 (Thomas et al., Reference Thomas, Laake, Derry, Buckland, Borchers and Burnham1998, Reference Thomas, Buckland, Rexstad, Laake, Strindberg and Hedley2010) to estimate orang-utan nest density. The software fits several possible robust, semi-parametric models to the data to determine the probability of detection as a function of the distance of the observed nest from the transect, or the effective strip width. The effective strip width was estimated regionally (across Block C). We selected a half-normal + cosine model key function/series expansion based on the lowest Akaike Information Criterion (AIC = 4,038.73). We divided the data into 10 equal intervals to smooth the histogram and improve the model (AIC = 2,620.34; probability of a greater χ 2 goodness-of-fit value, P = 0.19). Nest density was estimated locally (per patch) using the formula d n  = N/L × 2w, where d n is nest density (nests per km2), N is the number of observed nests per patch, taking into account a 30 m truncation, L is the sum of the lengths of the transects (in km) per patch, and w is the effective strip width (in km); variance was derived using analytical estimates. We assigned the regional nest density estimate to the patches that were not surveyed.

To estimate population density we used the formula of van Schaik et al. (Reference van Schaik, Priatna, Priatna, Nadler, Galdikas, Sheeran and Rosen1995): d o = d n /(p * r * t), where d o is orang-utan density (individuals per km2), d n is nest density, p is the proportion of nest-builders in the population, r is the rate at which nests are produced (nests per day per individual) and t is the decay rate of nests, or time during which a nest remains viable (days). Accurate values of p, r and t are vital for producing accurate density estimates (Marshall & Meijaard, Reference Marshall and Meijaard2009) and these values, particularly t, can vary considerably between field sites (van Schaik et al., Reference van Schaik, Priatna, Priatna, Nadler, Galdikas, Sheeran and Rosen1995, Reference van Schaik, Wich, Utami and Odom2005; Morrogh-Bernard et al., Reference Morrogh-Bernard, Husson, Page and Rieley2003; Mathewson et al., Reference Mathewson, Spehar, Meijaard, Nardiyono and Sasmirul2008). We used parameter values derived from the adjacent Sabangau Forest (p = 0.89, r = 1.17, t = 365.16 ± SE 8.76; Husson et al., Reference Husson, Wich., Marshall, Dennis, Ancrenaz, Brassey, Wich, Utami Atmoko, Mitra Setia and van Schaik2009), which is geographically close to, recently contiguous with, and ecologically similar to the Mega Rice Project area. We also included density estimates calculated using the full range of values reported for the parameters p, r and t in peat-swamp forests in Borneo (Table 3).

We estimated orang-utan numbers for each forest patch by extrapolating density estimates and the associated standard error to patch sizes derived from the satellite data. We applied a correction factor of 1.475, as suggested in Husson et al. (Reference Husson, Wich., Marshall, Dennis, Ancrenaz, Brassey, Wich, Utami Atmoko, Mitra Setia and van Schaik2009), to produce a standardized density estimate, which can be compared with standardized density estimates of other populations, calculated based on different survey methods. This correction factor accounts for depressed estimates of nest density based on a survey design in which line transects are surveyed only once, compared with line transects with a repeat survey technique or plots. To avoid overestimation we used our original uncorrected density estimates to calculate orang-utan numbers for each patch and extrapolate a minimum population estimate.

Results

According to the land cover/land use classification (Fig. 2) c. 10% of the area in Block C comprises peat-swamp forest (Table 1). This increases to 17% when degraded or secondary peat-swamp forest is included, which represents an area of 76,755 ha (Table 1), 67,718 ha of which comprises patches > 25 ha. The area of viable habitat (fragments > 250 ha) is 59,948 ha, distributed among 29 patches (Table 2).

Fig. 2 (a) Land cover/land use in Block C of the former Mega Rice Project in Central Kalimantan, Indonesia. (b) Habitat patches of > 250 hectares and estimated orang-utan population density within Block C.

Table 1 Land use/land cover in Block C of the Mega Rice Project, Central Kalimantan, Indonesia (Fig. 1), with land area and percentage of landscape.

Table 2 Patch area, mean orang-utan Pongo pygmaeus wurmbii density, and mean number of orang-utans in each patch > 250 ha in Block C of the Mega Rice Project, Central Kalimantan, Indonesia (Fig. 1). The regional density estimate (Block C-wide) is applied to the patches that were not surveyed directly.

The DISTANCE analysis indicates an effective strip width of 13.09 m for the survey, and a nest density estimate of 944.77 ± SE 103.07 km−2. Orang-utan density estimates based on the range of published values for the parameters p, r and t in peat-swamp forests in Borneo vary from 2.27 ± SE 0.25 to 2.56 ± SE 0.28 km−2 (Table 3). Using the values for p, r and t from Sabangau, the density estimate for Block C is 2.48 ± SE 0.32 individuals km−2 and the standardized density estimate is 3.66± ± SE 0.47 km−2. The density of orang-utans in the patches that were surveyed directly ranges from 1.61 ± SE 0.21 to 4.62 ± SE 0.60 km−2 (Fig. 2, Table 2). Based on patch-specific density estimates for the patches that were surveyed and the regional density estimate for the patches that were not, the population size over the entire Block C is 1,507 ± SE 195 to 1,700 ± SE 220 (Table 2), using 250 and 25 ha minimum patch size thresholds, respectively. It is thought that 250 individuals are a genetically viable population over the long term (Singleton et al., Reference Singleton, Wich, Husson, Stephens, Utami-Atmoro and Leighton2004), and none of the forest fragments support such a population, with the potential exception of patches 3 and 13, with 227 ± SE 29 and 232 ± SE 30 individuals, respectively (Table 2). However, none of these populations should be abandoned, as the larger landscape supports a large population, which highlights the importance of developing a management plan that incorporates orang-utan habitat connectivity in Block C.

Table 3 Orang-utan density estimates for Block C, based on the range of published values for the parameters p, r and t for peat-swamp forests in Borneo and the standard error associated with nest density in our dataset (but not our parameter estimates). The best estimates for parameter values for Block C of the Mega Rice Project yield an estimated density of 2.49 ± SE 0.27 individuals per km2.

1 Best estimates for parameter values for Block C of the Mega Rice Project

2 Husson (unpubl. data)

5 Morrogh-Bernard (unpubl. data)

Discussion

We identified the density and abundance of Bornean orang-utan subpopulations and quantified the remaining habitat area in Block C of the former Mega Rice Project to contribute to a more focused conservation effort for this population of c. 1,500–1,700 orang-utans.

Prior to the construction of irrigation canals in 1995–1996 Block C contained 233,275 ha of peat-swamp forest (Boehm & Siegert, Reference Boehm and Siegert2001). Since then c. 70% of the forest has been lost as a result of rapid forest fragmentation and subsequent drainage and fire, and the orang-utans have become confined to habitat fragments. The current population density may be temporarily inflated above the carrying capacity of the fragments, and therefore the population may be unable to persist in the long term because of this extinction debt (Tilman et al., Reference Tilman, May, Lehman and Nowak1994), as may also be the case in other areas that have experienced rapid loss of peat forest in recent history. Supporting this, our standardized density estimate of 3.66 ± SE 0.47 individuals km−2 for this site is relatively high compared to the adjacent Sabangau area, with a standardized density estimate of 1.12–2.49 individuals km−2 (Husson et al., Reference Husson, Wich., Marshall, Dennis, Ancrenaz, Brassey, Wich, Utami Atmoko, Mitra Setia and van Schaik2009).

Using a density estimate derived from an intact mixed swamp forest area adjacent to the Mega Rice Project (nest density estimate 599 ± SE 78 km−2; Morrogh-Bernard et al., Reference Morrogh-Bernard, Husson, Page and Rieley2003) as a pre-canal baseline, we estimate the original population in Block C to have been 3,676 ± SE 479 orang-utans, c. 55–60% of which have been lost. Unless the area of viable habitat increases, the population density will probably decrease further. If it decreases to 1.58 individuals km−2 (derived from an adjacent intact mixed swamp forest area; Morrogh-Bernard et al., Reference Morrogh-Bernard, Husson, Page and Rieley2003) the population on Block C would be reduced to 945 ± SE 123 (minimum patch size 250 ha) to 1,067 ± SE 139 (minimum patch size 25 ha) individuals, assuming no further loss of forest were to occur. This underscores the need to reforest barren areas and to connect existing forest fragments.

The effective conservation of this population will also require information concerning how orang-utan population ecology is affected by changes in habitat extent and spatial configuration. Although the effects of forest disturbance (e.g. logging) on orang-utan density and demography (Felton et al., Reference Felton, Engström, Felton and Knott2003; Morrogh-Bernard et al., Reference Morrogh-Bernard, Husson, Page and Rieley2003) and behaviour (Hardus et al., Reference Hardus, Lameira, Menken and Wich2012) have been documented, little is known about how orang-utans respond to a harsh non-forest matrix (e.g. barren or grassland areas) and how they use these non-forest areas, if at all. It is expected that they rarely disperse between forest fragments (van Schaik et al., Reference van Schaik, Monk and Robertson2001). This may not be the case in a multi-functional landscape, such as plantation matrix (Meijaard et al., Reference Meijaard, Albar, Nardiyono, Rayadin, Ancrenaz and Spehar2010) or mixed agroforestry systems (Campbell-Smith et al., Reference Campbell-Smith, Campbell-Smith, Singleton and Linkie2011a,Reference Campbell-Smith, Campbell-Smith, Singleton and Linkieb), but is probably the case in places such as the Mega Rice Project where the matrix is relatively harsh. However, if orang-utans traverse the matrix relatively frequently it is thought that small forest patches supplement the habitat area provided by larger patches. If we categorized all peat-swamp forest areas as habitat, the population estimate for Block C would increase to 1,925 ± SE 249.

We selected a 250 ha threshold for the minimum habitat patch size, based on the range requirements of female orang-utans (Singleton et al., Reference Singleton, Knott, Morrogh-Bernard, Wich, van Schaik, Wich, Atmoko, Setia and van Schaik2009). However, male home ranges are larger (Galdikas, Reference Galdikas1988; Nietlisbach et al., Reference Nietlisbach, Arora, Nater, Goossens, van Schaik and Krützen2012) and they are not exclusive or stable (van Schaik & van Hooff, Reference van Schaik, van Hooff, McGrew, Marchant and Nishida1996). Thus, the spatial distribution of habitat patches is especially important for dispersal of male orang-utans and the resulting genetic variation in individuals and connectivity between meta-populations across the landscape. More research on the movement patterns of orang-utans in a fragmented landscape is required (see Goossens et al., Reference Goossens, Chikhi, Jalil, Ancrenaz, Lackman-Ancrenaz and Mohamed2005, for the genetic effects of fragmentation).

The importance of this population to the persistence of the species regionally and globally is an issue of value judgement and prioritization. The population has limited potential to connect to other populations of orang-utans, as it became functionally isolated from populations in the Sabangau Forest with the development of the city of Palangka Raya. In terms of numbers this population accounts for c. 2–4% of the global total and 4–5% of the subspecies P. pygmaeus wurmbii (Wich et al., Reference Wich, Meijaard, Marshall, Husson, Ancrenaz and Lacy2008). However, every viable population contributes to the persistence of the species, and the Indonesian government has made a commitment to stabilize all populations of orang-utans and their habitat (Soehartono et al., Reference Soehartono, Susilo, Andayani, Atmoko, Sihite, Saleh and Sutrisno2007). Furthermore, this population is potentially the seventh largest population of P. pygmaeus wurmbii (Wich et al., Reference Wich, Meijaard, Marshall, Husson, Ancrenaz and Lacy2008). For this population to persist, direct conservation action in the area will be required, including closing the irrigation canals, reforesting barren areas and fighting fires. Although efforts are being made to restore Block C, they are small-scale, limited and underfunded and this scenario is likely to continue if land is designated for conversion and not conservation.

The loss of peat-swamp forest could potentially be slowed by climate mitigation policies that provide financial incentives for avoiding carbon emissions. Peatlands have a large capacity for below-ground carbon sequestration and storage and, thus, an effect on global carbon cycles and climate change (Sorensen, Reference Sorensen1993). The Oslo Pact (Solheim & Natalegawa, Reference Solheim and Natalegawa2010) was initiated in 2011, with a 2-year moratorium on new permits for the conversion or logging of carbon-rich deep peatlands (> 50 cm) and of primary forest (Presidential Instruction No. 10/2011). It was extended for an additional 2 years (Presidential Instruction No. 6/2013), which could benefit peat-swamp conservation, particularly in Block C, the majority of which is protected under the moratorium. If the moratorium is properly enforced and continually renewed it could have a significant effect on the area's capacity to support orang-utans in the long term. To evaluate the agreement's contribution to orang-utan conservation at the national scale it will be critical to determine to what extent the areas protected under the agreement overlap with orang-utan habitat.

In addition to supporting the moratorium we also recommend conserving the marginal, shallower peat zones that fall outside the protection of the moratorium. Management of these shallow areas is required to maintain water tables in the upslope, deep interior peat areas, and these are some of the areas in which orang-utan densities are highest. The highest priorities are to prevent further oxidation of peatlands, increase the quantity and connectivity of the forest for the resident population of orang-utans and decrease the likelihood of the detrimental peatland fires that have been occurring in this region since the 1990s.

Acknowledgements

We thank the Kuzmier–Lee–Nikitine Endowment Fund, the SIDG–Lazar Foundation, the Nicholas School International Internship Fund and the Orangutan Foundation for financial support for this project; Hendri and Ari Purwanto for research support; and Dean Urban and Jennifer Swenson of Duke University and two anonymous reviewers for helpful comments on this article. The Orangutan Tropical Peatland Project works in partnership with the Center for International Cooperation in Sustainable Management of Tropical Peatland and would like to thank the University of Palangka Raya for ongoing support, the Ministry of Research and Technology for permission to undertake research in Indonesia, and the Wallace Global Fund, the Arcus Foundation, the Australian Orangutan Project, Rufford Small Grants for Nature and the U.S. Fish & Wildlife Service Great Apes Conservation Fund for financial support.

Biographical sketches

Megan Cattau uses remote sensing, geospatial analysis and modelling to research the effects of human alteration of the landscape on ecosystem service provision and on the associated species drivers. She is interested in the patterns and processes of forest community change following habitat alteration in peat-swamp forest. Simon Husson has worked on orang-utan conservation in Kalimantan since 1999, with a special focus on surveying unknown populations throughout the island, protecting populations in peat-swamp forest, and the reintroduction of ex-captive orang-utans to the wild. Susan Cheyne has worked in Indonesia since 2002 and is leading a long-term study of gibbon behaviour and ecology in peat-swamp forest as well as carrying out a detailed study of felid biodiversity and conservation in the area. She has carried out surveys on flying-fox hunting and abundance and is interested in how anthropogenic factors affect biodiversity in peat-swamp forests.

References

Aldhous, P. (2004) Land remediation: Borneo is burning. Nature, 432, 144146.CrossRefGoogle ScholarPubMed
Ancrenaz, M., Marshall, A., Goossens, B., van Schaik, C., Sugardjito, J., Gumal, M. & Wich, S. (2008) Pongo pygmaeus. In IUCN Red List of Threatened Species v. 2010.1. Http://www.iucnredlist.org [accessed 20 December 2012].Google Scholar
Barr, C. (2002) Timber concession reform: questioning the “sustainable logging’ paradigm. In Which Way Forward? People, Forests, and Policymaking in Indonesia (eds Colfer, C.J.P. & Resosudarmo, I.A.P.), pp. 191220. Resources for the Future, Center for International Forestry Research (CIFOR) and Institute of Southeast Asian Studies (ISEAS), Washington, DC, USA.Google Scholar
Boehm, H.D.V. & Siegert, F. (1999) Application of remote sensing and GIS to survey and evaluate tropical peat. In The International Conference and Workshop on Tropical Peat Swamps: Safe-guarding a Global Natural Resource, pp. 341356. Kalteng Consultants, Penang, Malaysia.Google Scholar
Boehm, H.D.V. & Siegert, F. (2001) Ecological impact of the one million hectare rice project in Central Kalimantan, Indonesia, using remote sensing and GIS. In 22nd Asian Conference on Remote Sensing, 5–9 November 2001, Singapore, pp. 16. Centre for Remote Imaging, Sensing and Processing CRISP, National University of Singapore, Singapore Institute of Surveyors and Values SISV and Asian Association on Remote Sensing.Google Scholar
Buckland, S.T., Anderson, D.R., Burnham, K.P. & Laake, J.L. (1993) Distance Sampling: Estimating Abundance of Biological Populations. Chapman & Hall, London, UK.Google Scholar
Buckland, S.T., Anderson, D.R., Burnham, K.P., Laake, J.L., Borchers, D.L. & Thomas, L. (2001) Introduction to Distance Sampling: Estimating Abundance of Biological Populations. Oxford University Press, New York, USA.Google Scholar
Campbell-Smith, G., Campbell-Smith, M., Singleton, I. & Linkie, M. (2011a) Apes in space: saving an imperilled orangutan population in Sumatra. PLoS ONE, 6(2), e17210.CrossRefGoogle ScholarPubMed
Campbell-Smith, G., Campbell-Smith, M., Singleton, I. & Linkie, M. (2011b) Raiders of the lost bark: orangutan foraging strategies in a degraded landscape. PLoS ONE, 6(6), e20962.CrossRefGoogle Scholar
Felton, A.M., Engström, L.M., Felton, A. & Knott, C.D. (2003) Orangutan population density, forest structure and fruit availability in hand-logged and unlogged peat swamp forests in West Kalimantan, Indonesia. Biological Conservation, 114, 91101.Google Scholar
Fuller, D.O., Hardiono, M. & Meijaard, E. (2011) Deforestation projections for carbon-rich peat swamp forests of Central Kalimantan, Indonesia. Environmental Management, 48, 436447.Google Scholar
Galdikas, B.M.F. (1988) Orangutan diet, range, and activity at Tanjung Puting, Central Borneo. International Journal of Primatology, 9, 135.Google Scholar
Goossens, B., Chikhi, L., Jalil, M.F., Ancrenaz, M., Lackman-Ancrenaz, I., Mohamed, M. et al. (2005) Patterns of genetic diversity and migration in increasingly fragmented and declining orang-utan (Pongo pygmaeus) populations from Sabah, Malaysia. Molecular Ecology, 14, 441456.Google Scholar
Hardus, M.E., Lameira, A.R., Menken, S.B.J. & Wich, S.A. (2012) Effects of logging on orangutan behavior. Biological Conservation, 146, 177187.Google Scholar
Hooijer, A., Silvius, M., Wösten, H. & Page, S. (2006) PEAT–CO2, Assessment of CO2 emissions from drained peatlands in SE Asia. Delft Hydraulics report Q3943.Google Scholar
Husson, S.J., Wich., S.A., Marshall, A.J., Dennis, R.D., Ancrenaz, M., Brassey, R. et al. (2009) Orangutan distribution, density, abundance and impacts of disturbance. In Orangutans: Geographic Variation in Behavioral Ecology and Conservation (eds Wich, S.A., Utami Atmoko, S.S., Mitra Setia, T. & van Schaik, C.P.), pp. 7796. Oxford University Press, Oxford, UK.Google Scholar
Johnson, A.E., Knott, C.D., Pamungkas, B., Pasaribu, M. & Marshall, A.J. (2005) A survey of the orangutan (Pongo pygmaeus wurmbii) population in and around Gunung Palung National Park, West Kalimantan, Indonesia based on nest counts. Biological Conservation, 121, 495507.CrossRefGoogle Scholar
Koh, L.P., Miettinen, J., Liew, S.C. & Ghazoul, J. (2011) Remotely sensed evidence of tropical peatland conversion to oil palm. Proceedings of the National Academy of Sciences of the United States of America, 108, 51275132.Google Scholar
Kuhl, H., Maisels, F., Ancrenaz, M. & Williamson, E.A. (2008) Best Practice Guidelines for Surveys and Monitoring of Great Ape Populations. IUCN SSC Primate Specialist Group, Gland, Switzerland.CrossRefGoogle Scholar
Marshall, A.J. & Meijaard, E. (2009) Orang-utan nest surveys: the devil is in the details. Oryx, 43, 416418.Google Scholar
Mathewson, P.D., Spehar, S.N., Meijaard, E., Nardiyono, Purnomo, Sasmirul, A. et al. (2008) Evaluating orangutan census techniques using nest decay rates: implications for population estimates. Ecological Applications, 18, 208221.Google Scholar
Meijaard, E., Albar, G., Nardiyono, , Rayadin, Y., Ancrenaz, M. & Spehar, S. (2010) Unexpected ecological resilience in Bornean orangutans and implications for pulp and paper plantation management. PLoS ONE, 5(9), e12813.Google Scholar
Meijaard, E. & Wich, S. (2007) Putting orang-utan population trends into perspective. Current Biology, 17, R540.Google Scholar
Morrogh-Bernard, H., Husson, S., Page, S.E. & Rieley, J.O. (2003) Population status of the Bornean orang-utan (Pongo pygmaeus) in the Sebangau peat swamp forest, Central Kalimantan, Indonesia. Biological Conservation, 110, 141152.Google Scholar
Ng, P.K.L., Tay, J.B. & Lim, K.K.P. (1994) Diversity and conservation of blackwater fishes in Peninsular Malaysia, particularly in the North Selangor peat swamp forest. Hydrobiologia, 285, 203218.Google Scholar
Nietlisbach, P., Arora, N., Nater, A., Goossens, B., van Schaik, C.P. & Krützen, M. (2012) Heavily male-biased long-distance dispersal of orang-utans (genus: Pongo), as revealed by Y-chromosomal and mitochondrial genetic markers. Molecular Ecology, 21, 31733186.Google Scholar
Page, S.E. & Rieley, J.O. (1998) Tropical peatlands: a review of their natural resource functions. with particular reference to Southeast Asia. International Peat Journal, 8, 95106.Google Scholar
Page, S.E., Rieley, J.O. & Wüst, R. (2006) Lowland tropical peatlands of Southeast Asia. In Peatlands: Evolution and Records of Environmental and Climate Changes (eds Martini, I.P., Martínez Cortizas, A. & Chesworth, W.), pp. 145172. Elsevier, Amsterdam, The Netherlands.Google Scholar
Page, S.E., Siegert, F., Rieley, J.O., Boehm, H.-D.V., Jaya, A. & Limin, S. (2002) The amount of carbon released from peat and forest fires in Indonesia during 1997. Nature, 420, 6165.Google Scholar
Rijksen, H.D. & Meijaard, E. (1999) Our Vanishing Relative: The Status of Wild Orang-utans at the Close of the Twentieth Century. Kluwer Academic Publishers, Dordrecht, The Netherlands.Google Scholar
Sabiham, S. (2004) Ecological issues of the Mega-Rice Project in Indonesia: a case study of swampland development in Central Kalimantan. In Ecological Destruction, Health, and Development; Advancing Asian Paradigms (eds Furukawa, H., Nishibuchi, M., Kono, Y. & Kaida, Y.), pp. 7387. Kyoto University Press, Kyoto, Japan.Google Scholar
Singleton, I., Knott, C.D., Morrogh-Bernard, H., Wich, S. & van Schaik, C. (2009) Ranging behavior of orangutan females and social organization. In Orangutans: Geographic Variation in Behavioral Ecology and Conservation (eds Wich, S.A., Atmoko, S.S.Utami, Setia, T.Mitra & van Schaik, C.), pp. 205212. Oxford University Press, Oxford, UK.Google Scholar
Singleton, I., Wich, S.A., Husson, S., Stephens, S., Utami-Atmoro, S.S., Leighton, M. et al. (2004) Orangutan Population and Habitat Viability Assessment: Final Report. IUCN/SSC Conservation Breeding Specialist Group, Apple Valley, USA.Google Scholar
Sodhi, N.S., Koh, L.P., Brook, B.W. & Ng, P.K.L. (2004) Southeast Asian biodiversity: an impending disaster. TRENDS in Ecology & Evolution, 19, 654660.Google Scholar
Soehartono, T., Susilo, H.D., Andayani, N., Atmoko, S.S.U., Sihite, J., Saleh, C. & Sutrisno, A. (2007) Strategi dan Rencana aksi Konservasi Orangutan Indonesia 2007–2017 (ed. Direktorat Jenderal Perlindungan Hutan dan Konservasi Alam). Departemen Kehutanan Republik Indonesia, Jakarta, Indonesia.Google Scholar
Solheim, E. & Natalegawa, R.M.M.M. (2010) Letter of intent between the Government of the Kingdom of Norway and the Government of the Republic of Indonesia on cooperation on reducing greenhouse gas emissions from deforestation and forest degradation. Oslo, Norway.Google Scholar
Sorensen, K.W. (1993) Indonesian peat swamp forests and their role as a carbon sink. Chemosphere, 27, 10651082.Google Scholar
Thomas, L., Buckland, S.T., Rexstad, E.A., Laake, J.L., Strindberg, S., Hedley, S.L. et al. (2010) Distance software: design and analysis of distance sampling surveys for estimating population size. Journal of Applied Ecology, 47, 514.Google Scholar
Thomas, L., Laake, J.L., Derry, J.F., Buckland, S.T., Borchers, D.L., Burnham, K.P. et al. (1998) DISTANCE v. 6.0. Research Unit for Wildlife Population Assessment, University of St Andrews, UK.Google Scholar
Tilman, D., May, R.M., Lehman, C.L. & Nowak, M.A. (1994) Habitat destruction and the extinction debt. Nature, 371, 6566.Google Scholar
van Schaik, C.P., Monk, K.A. & Robertson, J.M.Y. (2001) Dramatic decline in orang-utan numbers in the Leuser Ecosystem, Northern Sumatra. Oryx, 35, 1425.Google Scholar
van Schaik, C.P., Priatna, A. & Priatna, D. (1995) Population estimates and habitat preferences of orangutans based on line transects of nests. In The Neglected Ape (eds Nadler, R.D., Galdikas, B.F.M., Sheeran, L.K. & Rosen, N.), pp. 129147. Plenum Press, New York, USA.Google Scholar
van Schaik, C.P. & van Hooff, J.A.R.A.M. (1996) Toward an understanding of the orangutan's social system. In Great Ape Societies (eds McGrew, W.C., Marchant, L.F. & Nishida, T.), pp. 315. Cambridge University Press, Cambridge, UK.Google Scholar
van Schaik, C.P., Wich, S.A., Utami, S.S. & Odom, K. (2005) A simple alternative to line transects of nests for estimating orangutan densities. Primates, 46, 249254.Google Scholar
Wich, S.A., Gaveau, D., Abram, N., Ancrenaz, M., Baccini, A., Brend, S. et al. (2012) Understanding the impacts of land-use policies on a threatened species: is there a future for the Bornean orang-utan? PLoS ONE, 7(11), e49142.Google Scholar
Wich, S.A., Meijaard, E., Marshall, A.J., Husson, S., Ancrenaz, M., Lacy, R.C. et al. (2008) Distribution and conservation status of the orang-utan (Pongo spp.) on Borneo and Sumatra: how many remain? Oryx, 42, 329339.Google Scholar
Williams, N. (2007) Orang-utan extinction threat shortens. Current Biology, 17, R261.Google Scholar
Yule, C. (2010) Loss of biodiversity and ecosystem functioning in Indo-Malayan peat swamp forests. Biodiversity and Conservation, 19, 393409.Google Scholar
Figure 0

Fig. 1 Block C of the former Mega Rice Project in Central Kalimantan, Indonesia, including locations of orang-utan Pongo pygmaeus nests along survey transects.

Figure 1

Fig. 2 (a) Land cover/land use in Block C of the former Mega Rice Project in Central Kalimantan, Indonesia. (b) Habitat patches of > 250 hectares and estimated orang-utan population density within Block C.

Figure 2

Table 1 Land use/land cover in Block C of the Mega Rice Project, Central Kalimantan, Indonesia (Fig. 1), with land area and percentage of landscape.

Figure 3

Table 2 Patch area, mean orang-utan Pongo pygmaeus wurmbii density, and mean number of orang-utans in each patch > 250 ha in Block C of the Mega Rice Project, Central Kalimantan, Indonesia (Fig. 1). The regional density estimate (Block C-wide) is applied to the patches that were not surveyed directly.

Figure 4

Table 3 Orang-utan density estimates for Block C, based on the range of published values for the parameters p, r and t for peat-swamp forests in Borneo and the standard error associated with nest density in our dataset (but not our parameter estimates). The best estimates for parameter values for Block C of the Mega Rice Project yield an estimated density of 2.49 ± SE 0.27 individuals per km2.