24 Jul 2014: The PLOS ONE Staff (2014) Correction: Chimpanzees Preferentially Select Sleeping Platform Construction Tree Species with Biomechanical Properties that Yield Stable, Firm, but Compliant Nests. doi: info:doi/10.1371/journal.pone.0104024 View correction
The daily construction of a sleeping platform or “nest” is a universal behavior among large-bodied hominoids. Among chimpanzees, most populations consistently select particular tree species for nesting, yet the principles that guide species preferences are poorly understood. At Semliki, Cynometra alexandri constitutes only 9.6% of all trees in the gallery forest in which the study populations ranges, but it was selected for 73.6% of the 1,844 chimpanzee night beds we sampled. To determine whether physical properties influence nesting site selection, we measured the physical characteristics of seven common tree species at the Toro-Semliki Wildlife Reserve, Uganda. We determined stiffness and bending strength for a sample of 326 branches from the seven most commonly used tree species. We selected test-branches with diameters typically used for nest construction. We measured internode distance, calculated mean leaf surface area (cm2) and assigned a tree architecture category to each of the seven species. C. alexandri fell at the extreme of the sample for all four variables and shared a tree architecture with only one other of the most commonly selected species. C. alexandri was the stiffest and had the greatest bending strength; it had the smallest internode distance and the smallest leaf surface area. C. alexandri and the second most commonly selected species, Cola gigantea, share a ‘Model of Koriba’ tree architecture. We conclude that chimpanzees are aware of the structural properties of C. alexandri branches and choose it because its properties afford chimpanzees sleeping platforms that are firm, stable and resilient.
Citation: Samson DR, Hunt KD (2014) Chimpanzees Preferentially Select Sleeping Platform Construction Tree Species with Biomechanical Properties that Yield Stable, Firm, but Compliant Nests. PLoS ONE 9(4): e95361. doi:10.1371/journal.pone.0095361
Editor: Sarah Frances Brosnan, Georgia State University, United States of America
Received: December 21, 2013; Accepted: March 25, 2014; Published: April 16, 2014
Copyright: © 2014 Samson, Hunt. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: National Science Foundation (SGER BNS 97-11124 and BCS 98-15991) and Indiana University (Faculty Research Support Program and the College of Arts and Sciences. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Juvenile and adult apes devote considerable time and energy to the construction of a new sleeping platform or “nest” at the end of their daily active period . Current data suggests that infants and young juveniles (i.e. nursing young) acquire skills over years both through observation of their mother and practice – and begin making their own nests after weaning. The universality of sleeping platform construction among the great apes suggests the behavior is genetically predisposed, though observation and learning are known to be critical . Nest-builders must select an appropriate site, climb to the site and manipulate a large volume of foliage while maintaining balance. They bend and break stiff, strong stems ,  as they incorporate foliage into the nest structure, pulling nest material inwards and interweaving it into a thick, springy ‘mattress,’ often bending branches in two. Ape nest mattresses are functionally concave in that either the edges are elevated over the mattress surface or the edges are less compliant than the center , causing the nest to assume a concave surface under pressure.
The function of sleeping platforms seems straightforward: a compliant yet constraining structure reduces stress on tissues and the functional concavity of the nests obviates the need to adjust posture during sleep to prevent falls. This sleep quality hypothesis holds that apes construct sleeping platforms to allow uninterrupted sleep and to promote longer individual sleep stages, resulting in a higher sleep quality , –. Additionally, captive orangutans exhibit higher quality sleep with less gross-motor movements and greater overall sleep times when using complex sleeping platforms . The evidence for the sleep quality hypothesis seems compelling, yet observations of patterns of nest site selection, nest heights and the physical characteristics of the most-preferred tree species are taken by some researchers as supporting a different function for nesting (although these hypotheses need not be mutually exclusive), including predation avoidance , , postural stability (preventing falls assumed to be more likely because apes have great body mass relative to local supporting branch diameter , ), thermoregulation , , , and pathogen avoidance–either because the nest serves as a physical barrier to insect vectors such as mosquitoes , ,  or because some chemical property of the species selected for nesting discourages mosquitoes , . In accord with predation avoidance, chimpanzees appear to select sites both as far from the main stem or trunk as possible and with an escape route to neighboring trees due to canopy connectivity , . In accord with the sleep quality hypothesis, tree species with smaller leaves and/or denser leaf distribution are argued to be selected to reduce stress on pressure points thus affording ‘comfort’  and potentially effect thermoregulation . Tree morphology may influence site selection because particular branching patterns such as the inverted tripod form is most easily manipulated into a bowl-shaped nest; chimpanzee preference at Bwindi for Drypetes gerrardii is hypothesized to be related to its “lollipop” crown shape and tripod morphology . Furthermore, tree morphologies may be reinforced through time by way of long term re-use of trees, which shapes local branch ‘morphologies’ of potential sleep sites .
To the extent that tree species vary in morphology, physical characteristics such as stiffness and habitat preference, functional imperatives are expected to be expressed in the selection of particular tree species as sleeping sites. If the sleep quality hypothesis is correct, chimpanzees should prefer species that have smaller leaves, denser canopies and tripod-shaped branchings, compared to other available species. It follows from the thermoregulation hypothesis that species with dense, leafier canopies would be preferred. The predator-avoidance hypothesis entails a preference for tree species that are tall, are characterized by broad canopies and are distributed near waterways or gorges because slopes increase the functional height of nests. The antivector hypothesis suggests that species with certain volatile compounds in bark, sap or leaves will be preferentially selected.
Branch diameters of supporting structures have been shown to be an essential variable for understanding sleep site selection and canopy movement in orangutans, as local diameter is negatively related to compliance and positively related to length of the trunk . Furthermore, is has been suggested that orangutans choose nest sites that afford stem diameters that yield optimal nest characteristics and that they manipulate nest materials in specific ways that demonstrate technical knowledge concerning structural properties of stems. Orangutan sleeping platforms have a high proportion of “greenstick fractures,” which are purported to impart a stronger and more resilient quality to supporting branches, suggesting that orangutans purposely break branches in this fashion during nest construction . Semliki chimpanzee tree-species preference may indicate that chimpanzees display technical knowledge of the physical properties of raw materials similar to that of orangutans and that it leads them to choose particular species for nesting. Eastern chimpanzees (Pan troglodytes schweinfurthii) at three relatively dry sites (Ishaha , Budongo  and Toro-Semliki ) in western Uganda strongly prefer the species Cynometra alexandri (C.H.Wright) as raw material for sleeping platform construction. C. alexandri is common in dry or riverine forests throughout Central and East Africa  where the wood is often known locally as ‘ironwood’ or ‘muhindi’ in recognition of its dense, durable and resilient qualities; it is useful as a construction material . Here we compare the structural qualities of seven common species of trees at Semliki to determine whether chimpanzees purposely select tree species that possess mechanical properties that determine superior nesting qualities.
A body mass of 30 kg or more means that chimpanzees require strong materials to contain their center of mass during sleep phases with a period of physical paralysis . Furthermore, it is expected that materials with great stiffness would be preferred for construction of a springy mattress that can bear weight without over-compressing thus allowing contact with inflexible and uncomfortable large-diameter supports. If the physical properties of trees influence nesting site selection, we predict that the trees most commonly selected by chimpanzees will have significantly greater strength (capacity to bear stress before catastrophic failure), a higher elastic modulus or stiffness, significantly smaller internode distances (correlated with stiffness), tree architecture characterized by a high proportion of inverted tripod branchings and/or small leaf surface areas.
Authorization to conduct research inside Uganda was granted by the Government of Uganda. Permission to carry out research at the Toro-Semliki Wildlife Reserve was granted and approved through permits from the Uganda Wildlife Authority (UWA) and the National Research Council.
The Toro-Semliki Wildlife Reserve (TSWR) occupies 548 km2 in the Great Rift Valley from the Semliki River in the west to the top of the escarpment in the east, and from the foothills of the Ruwenzori Mountains in the south to the shore of Lake Albert in the north, northwest of Fort Portal, Uganda (0°50′ to 1°05′N, 30°20′ to 30°35′ E). The Wasa River runs from south to north through the center of the reserve, emptying into Lake Albert in the north. The reserve is crosscut by small, shallow, often seasonal water-courses that support narrow gallery forests ranging in width from 50–250 m . The chimpanzee study community occupies the Mugiri River valley and eastwards up the escarpment slope to include valleys and seasonal tributaries to the Mugiri and the open woodland, bushland and grassland between the water-course; the community home range is the largest known of any site  and has been calculated to be 96 km2 (minimum convex polygon). The biome is predominantly dry Combretum and Borassus palm grassland with only 7.25% forest cover . The habitat is hot and dry, with a daily maximum averaging 34°C and an average rainfall of 1389 mm (1996–2012), though earlier rainfall records vary between 700 and 1300 mm , . The Mugiri community may have 150 members; 29 males have been identified, but few females are known as individuals; however, typical chimpanzee demography yields 60 females and 60 immatures .
Sleeping Platform Tree Species
Phenology data on tree species distribution throughout the habitat was used from previous work . Chimpanzee sleeping platforms were noted during the course of regular behavioral observation. Typical variables were recorded for each nest, including the species in which the nest was found. N = 1844 nests were included in the sample.
Tree Architecture Classification
We followed van Wyk and colleagues  in assigning tree species used for nesting to one of 23 architectural model categories. Tree architecture is classified according to the developmental sequence of axes, or shoots . Six tree architecture models were used for nest construction at Semliki (with associated prevalence throughout the home range): Model of Attim (9.9%), Model of Fagerlind (5.3%), Model of Koriba (58.2%), Model of Leeuwenberg (10.4%), Model of Tomlinson (4.4%), and Model of Troll (0.4%). We used X2 analysis to assess chimpanzee preference for architectural models, relative to prevalence within the home range.
Material Properties Measurement
Our methods closely followed Stewart and colleagues  by determining the biomechanical propeties of stems (a primary plant axis that develops buds and shoots instead of roots). Three-hundred and twenty six stems were used from the same multiple species generated in a sample of 65 nests from May–June 2008 and August 2010–January 2011; samples closely conformed to the length and diameter of “frame support branches” in nests (FSB diameter [N = 60, 4.13 cm ±1.11], see 9); FSB’s are branches that have been bent double and interwoven in the initial stages of nest construction and are used as primary weight bearing supports. The force in kg required to bend stems to 45°, 90° and to the point of structural failure were measured with a spring balance. We used the point of attachment of the spring balance and the distance from the anchor point to the break point to calculate torque, equal to the force applied multiplied by the distance between an object’s axis of rotation and the point where the force is applied . A relative break force (RBF) value was calculated using a standardized measure of the force necessary to break any branch at a distance of 1 m. The RBF values were used to assess bending strength across tree species (One-way ANOVAs). Beilschmiedia ugandensis was an ideal control given its rare selection as a sleeping site and ubiquity throughout the home range and was featured in a LSD post hoc analysis of the RBF values compared among preferred species.
We measured internode lengths (N = 2574) along the stems of selected tree species often selected for sleeping sites to compare internode distances among genera (One-way ANOVA), using Beilschmiedia ugandensis as a control. We calculated the surface area of leaves (N = 428) from selected tree species by tracing leaf outlines over 1 cm2 paper (then summing the number of squares within the outline) and compared species using a one-way ANOVA, again with B. ugandensis used as a control.
All statistical tests were 2-tailed, set at an alpha = 0.05 significance level.
Of 1,844 nests sampled, Cynometra alexandri was selected for 73.6% of the nests, even though it represents only 9.6% of all trees on our 20 habitat-sampling transects (Fig. 1, ); this value is the second strongest preference for sleeping tree species recorded to date among all chimpanzee sites (Table 1). The second most commonly selected tree species at Semliki was Cola gigantea, constituting 9.2% of all recorded nests, but representing only 0.9% tree species in the habitat. The most common species sampled on our transects was Beilschmiedia ugandensis, representing 42.3% of all tree species. This most-common species was selected for nesting only 16 times, making up only 0.8% of all nests. Other species selected for nesting were Albizia grandibracteata, Combretum molle, Ficus mucuso, Phoenix reclinata and Pseudospondias microcarpa.
In a one-way ANOVA test C. alexandri was the stiffest and most stress resistant of the eight species we tested, with the highest relative break force (RBF) greater than the other seven species in three of four diameter categories (see Table 2 for RBF distributions and Table 3 for post hoc analysis), category 1, <3 cm (F [6, 199]) = 11.49, P<0.001), category 2, 3–4.9 cm (F [6, 155] = 6.41, P<0.001), category 3, 5–6.9 cm (F [6, 50] = 10.80, P<0.001). Size category 4, 7–9 cm, (F ,  = 0.84, P = 0.524) did not differ significantly from other species; however, our sample contained very few branches in this diameter category (Table 2).
In a one-way ANOVA, C. alexandri had significantly smaller internode distances compared to seven comparison species (N = 150, 1.47±1.3 cm, range: 0–9; F [6, 1219] = 13.20, P<0.001). In a one-way ANOVA C. alexandri had significantly smaller leaf surface areas than other species (N = 83, 3.77±2.9 cm, range: 0.25–18; F [4, 240] = 140.31, P<0.001). The second most commonly selected tree species, C. gigantea, had the largest leaf surface area (N = 33, 208.14±112.4 cm, range: 17.5–426.25).
Of the seven architectural models characterizing trees in the TSWR, four were commonly used by chimpanzees: Model of Troll (characteristic of Albizia; N = 120); Model of Leewenberg (both Combretum [N = 24] and Ficus [N = 30]); Model of Tomlinson (Phoenix [N = 70]); Model of Koriba (Cynometra [N = 1430], Cola [N = 189], and Pseudospondias [N = 19]). Koriba was the most preferred tree architecture, selected for 90.0% of all trees, significantly greater than expected by chance (X2 = 1013.9, df = 6, P<0.001; see Table 4).
Our results strongly suggest that just as do orangutans , chimpanzees are selective of tree species when considering where to sleep. These data further suggest that chimpanzees select species of trees that possess physical properties that result in nests that are sturdy and resilient, optimizing comfort and reducing the risk of falls. The preferred species at Semliki, C. alexandri has the greatest relative break force and the smallest internode distance of the species tested; both promote stiffness. Because sleeping platforms utilize the basketweave (a variation of the plain weave [the most fundamental type of weave with a simple crisscross pattern] in which two are more stems can be bundled and then woven as one) , smaller internode distances may also introduce a greater number of interlocking points, yielding greater structurally integrity and resilience. Future research directions should investigate the mechanisms by which chimpanzees consider the physical properties of stems during platform construction and whether weaving patterns produce biomechanically sturdier sleeping platforms.
C. alexandri had the smallest leaves with the greatest density (i.e., internode distance) of all nesting tree-species, which has been suggested as affording the greatest comfort  by reducing exposure to branches protruding from the nest structure and increasing friction among interlocking of stems, creating a tighter, more securely woven structure. By providing thicker foliage, it may also increase insulation and thus offer thermoregulatory advantages. Finally, C. alexandri may also have insect-repellent properties .
Among the preferred tree species at Semliki (Fig. 1) was Phoenix reclinata, a palm with physical characteristics dramatically different from the most-preferred species. P. reclinata has pinnate, or feather-shaped leaves 3–5 cm in breadth and 40 cm in length. The leaves are stiff and the base of the leaf stem has thorns that incorporate paralytic secondary compounds . Use of palms for nest manufacture is common and highly preferred at some sites (refs. in Table 1); palms are the preferred species in southern Guinea-Bissau . We consider the selection of this species to be at odds with most hypotheses for nest construction: it rarely interdigitates with other canopies; it has no lateral branches; it is a short tree (relative to other nesting species); leaves are large; and interweaving is difficult. Sousa and colleagues  hypothesized that oil palm are selected for their antipredator qualities including increased line of sight (given the spatial location of oil palm was significantly situated at forest edge), increased communication possibilities with conspecifics and improved access to resources. We additionally hypothesize that the paralytic secondary compounds associated with thorny leaf stems and protruding, jagged trunk morphology attribute the antipredition characteristics associated with this species. Furthermore, it may be that oil palm is preferred because if affords maximal stiffness in substrate, given it is characterized by having no lateral branches and the weight bearing structure is the trunk itself.
Our results are compatible with the hypothesis that chimpanzees select trees that are configured similar to the lollipop morphology of Drypetes gerrardii . The model of Koriba C. alexandri tree architecture affords chimpanzees inverted-tripod nest frames, which are hypothetically the easiest to transform into the functionally concave form to maximize comfort and safety . Other species selected less preferentially than C. alexandri likewise support this hypothesis: three of the four (96.2% of all selected species) tree architectures used by chimpanzees at Semliki possess inverted tripod branching patterns (Fig. 2). The tree architecture Tomlinson is a unique case, as it is an oil-palm tree with a markedly different shoot development.
Notice the shoot development which produces a node dense, leafy and sturdy substrate with multiple frame supporting branches (FSBs) with which to construct a sleeping platform. In contrast, the shoot development which produces lateral drooping (inferred low levels of stiffness) and long internode distances illustrated by Model of Champagnat (below right corner), provides a poor sleeping substrate and is never selected by Semliki chimpanzees. Models Koriba, Troll and Leeuwenberg comprise 96.2% of all selected species and share the “lollipop” end static tree shape (adapted from ).
Our results suggest that the ideal sleeping platform tree species might well possess multiple advantages, perhaps possessing antipredator, antivector, thermoregulatory and comfort- maximizing qualities all at once. C. alexandri has all of these properties, suggesting that chimpanzees are keen observers of physical properties of trees, including stiffness, strength and leaf surface area, and that they select species that provide the widest range of advantages, including predator avoidance, postural stability, thermoregulation and pathogen avoidance.
We are grateful to the Government of Uganda, the Uganda Wildlife Authority and the National Research Council. We are grateful to the staff at the Semliki Chimpanzee Project, particularly Moses Comeboy. H. Green commented helpfully on the manuscript. S. Dickinson and the Indiana Statistical Consulting Center (ISCC) advised us on statistical methods.
Conceived and designed the experiments: DRS. Performed the experiments: DRS. Analyzed the data: DRS KDH. Contributed reagents/materials/analysis tools: DRS KDH. Wrote the paper: DRS KDH.
- 1. Goodall JM (1962) Nest building behavior in the free ranging chimpanzee. Ann. New York Acad Sci 102: 445–467. doi: 10.1111/j.1749-6632.1962.tb13652.x
- 2. Goodall J (1968) The behaviour of free-living chimpanzees in the Gombe Stream Reserve. Anim Behav Monogr 1(3): 165–311.
- 3. Videan EN (2006) Bed-building in captive chimpanzees (Pan troglodytes): The Importance of early rearing. Am J Primatol 68: 745–751. doi: 10.1002/ajp.20265
- 4. Stewart FA, Pruetz JD, Hansell MH (2007) Do chimpanzees build comfortable nests? Am J Primatol 69: 930–939. doi: 10.1002/ajp.20432
- 5. Videan EN (2005) Sleep and sleep-related behaviors in chimpanzee (Pan troglodytes). PhD (Miami University, Oxford, OH) p.93.
- 6. Fruth B, Hohmann G (1996). Nest building behavior in the great apes: The great leap forward? Great Ape Societies, eds McGrew WC, Marchant LF, Nishida T (Cambridge Univ Press: Cambridge), 225–240.
- 7. McGrew WC (2004) The Cultured Chimpanzee: Reflections on Cultural Primatology. (Cambridge Univ Press: New York) p 248.
- 8. Stewart FA (2011) Brief Communication: Why Sleep in a Nest? Empirical Testing of the Function of Simple Shelters Made by Wild Chimpanzees. Am J Phys Anthropol 146: 313–318. doi: 10.1002/ajpa.21580
- 9. Samson DR (2012) The chimpanzee nest quantified: morphology and ecology of arboreal sleeping platforms within the dry habitat site of Toro-Semliki Wildlife Reserve, Uganda, Primates. 53: 357–364. doi: 10.1007/s10329-012-0310-x
- 10. Samson DR, Shumaker RW (2013) Documenting orang-utan sleep architecture: sleeping platform complexity increases sleep quality in captive Pongo. Behaviour 150: 845–861. doi: 10.1163/1568539x-00003082
- 11. Stewart FA, Pruetz JD (2013) Do chimpanzee nests serve an anti-predatory function? Amer J Primatol 75(6): 593–604. doi: 10.1002/ajp.22138
- 12. Pruetz JD, Fulton SJ, Marchant LF, McGrew WC, Waller MSM (2008) Arboreal nesting as anti-predator adaptation by savanna chimpanzees (Pan troglodytes verus) in southeastern Senegal. Am J Primatol 70: 393–401. doi: 10.1002/ajp.20508
- 13. Baldwin PJ, Sabater Pi J, McGrew WC, Tutin CEG (1981) Comparisons of nests made by different populations of chimpanzees (Pan troglodytes). Primates 22: 474–486. doi: 10.1007/bf02381239
- 14. Koops K, McGrew WC, de Vries H, Matsuzawa T (2012) Nest-building by chimpanzees (Pan troglodytes verus) at Seringbara, Nimba Mountains: antipredation, thermoregulation, and antivector hypotheses. Int J Primatol 33: 356–380. doi: 10.1007/s10764-012-9585-4
- 15. Nunn CL, Heymann EW (2005) Malaria Infection and Host Behavior: A Comparative Study of Neotropical Primates. Beh Ecol Sociobiol 59: 30–37. doi: 10.1007/s00265-005-0005-z
- 16. Samson DR, Muehlenbein MP, Hunt KD (2011) Do chimpanzees (Pan troglodytes schweinfurthii) exhibit sleep related behaviors that minimize exposure to parasitic arthropods? A preliminary report on the possible anti-vector function of chimpanzee sleeping platforms. Primates 54: 73–80. doi: 10.1007/s10329-012-0329-z
- 17. Anderson JR (1984) Ethology and ecology of sleep in monkeys and apes. Adv Study Behav 14: 165–229. doi: 10.1016/s0065-3454(08)60302-2
- 18. Fruth B, Hohmann G (1993) Ecological and behavioural-aspects of nest-building in wild bonobos (Pan paniscus). Ethology 94: 113–126. doi: 10.1111/j.1439-0310.1993.tb00552.x
- 19. Stanford CB, O’Malley RC (2008) Sleeping tree choice by Bwindi chimpanzees. Am J Primatol 70: 642–649. doi: 10.1002/ajp.20539
- 20. Stewart FA, Piel AK, McGrew WC (2011) Living archaeology: artefacts of specific nest site fidelity in wild chimpanzees. J Hum Evol 61: 388–395. doi: 10.1016/j.jhevol.2011.05.005
- 21. van Casteren A, Sellers WI, Thorpe SKS, Coward S, Crompton RH, Myatt JP, Ennos AR (2012) Nest-building orangutans demonstrate engineering know-how to produce safe, comfortable beds. Proc Nat Acad Sci 109: 6873–6877. doi: 10.1073/pnas.1200902109
- 22. van Casteren A, Sellers WI, Thorpe SKS, Coward S, Cromton RH, Ennos AR (2013) Factors affecting the compliance and sway properties of tree branches used by the Sumatran orangutan (Pongo abelii). PLoS ONE 8: e67877. doi: 10.1371/journal.pone.0067877
- 23. Sept JM (1992) Was there no place like home? A new perspective on early hominid archaeological sites from the mapping of chimpanzee nests. Curr Anthropol 33: 187–207. doi: 10.1086/204050
- 24. Brownlow AR, Plumptre AJ, Reynolds V, Ward R (2001) Sources of variation in the nesting behavior of chimpanzees (Pan troglodytes schweinfurthii) in the Budongo Forest, Uganda. Am J Primatol 551: 49–55. doi: 10.1002/ajp.1038
- 25. Hunt KD, McGrew WC (2002) Chimpanzees in dry habitats at Mount Assirik, Senegal and at the Semliki-Toro Wildlife Reserve, Uganda, Behavioural Diversity in Chimpanzees and Bonobos, eds Boesch C, Hohmann G, and Marchant LF (Cambridge Univ Press: Cambridge) 35–51.
- 26. Plumptre AJ (2010) Long term changes in Africa’s Rift Valley: impacts on biodiversity and ecosystem (Nova Science Publishers).
- 27. Chudnoff M (1984) Tropical Timbers of the World. USDA Forest Service.
- 28. Samson DR, Hunt KD (2012) A Thermodynamic Comparison of Arboreal and Terrestrial Sleeping Sites for Dry-Habitat Chimpanzees (Pan troglodytes schweinfurthii) at the Toro-Semliki Wildlife Reserve, Uganda. Am J Primatol 4: 811–818. doi: 10.1002/ajp.22031
- 29. Pratt DJ, Gwynne MD, Blackie JR (1977) Rangeland management and ecology in east Africa (Hodder and Stoughton, London) 310.
- 30. Stumpf R (2007) Chimpanzees and bonobos: diversity within and between species, Primates in Perspective, (eds) Campbell CJ, Fuentes A, MacKinnon KC, Panger M, Bearder SK (Oxford University Press: New York) 321–344.
- 31. van Wyk B, van Wyk BE, van Wyk P (2002) Photographic Guide to Trees of Southern Africa. Wissenschaftliche Verlagsges: Broschiert.
- 32. Kadolph SJ (2007) Textiles, 10th ed. Saddle River, New Jersey, Pearson/Prentice-Hall.
- 33. Palgrave KC (1977) Trees of Southern Africa. C. Struik Publ.: Capetown.
- 34. Sousa J, Barata AV, Sousa C, Casanova CCN, Vicente L (2011) Chimpanzee Oil-Palm Use in Southern Cantanhez National Park, Guinea-Bissau. Am J Primatol 73: 485–497. doi: 10.1002/ajp.20926
- 35. Ogunjemite BG, Ashimi TA, Okeyoyin OA (2010) The chimpanzee community of German-Fort, and the potentials for the development of tourism-base management of Gashaka-Gumti National Park, Nigeria. J Sustain Develop Africa 12: 107–115.
- 36. Humle T (2003) Culture and variation in wild chimpanzee behaviour: a study of three communities in West Africa. PhD diss (University of Sterling, Scotland, UK).
- 37. Sanz C, Morgan D, Strindberg S, Onononga JR (2007) Distinguishing between the nests of sympatric chimpanzees and gorillas. J Appl Eco 44(2): 263–272. doi: 10.1111/j.1365-2664.2007.01278.x
- 38. Sept J (1998) Shadows on a changing landscape: comparing nesting patterns of hominids and chimpanzees since their last common ancestor. Amer J Primatol 46(1): 85–101. doi: 10.1002/(sici)1098-2345(1998)46:1<85::aid-ajp7>3.3.co;2-1
- 39. Basabose AK, Yamagiwa J (2002) Factors affecting nesting site choice in chimpanzees at Tshibati, Kahuzi-Biega National Park: influence of sympatric gorillas. Int J Pramatol 23(2): 263–282.
- 40. Petre CA, Hynen MC, Beudels-Jamar R (2007) First assessment of chimpanzee (Pan troglodytes troglodytes) density and bedding behaviour in the Pongara National Park, Gabon. Pan Africa News 14(2): 22–27.
- 41. Mulavwa MN (2010) Nest groups of wild bonobos at Wamba: selection of vegetation and tree species and relationships between nest group size and party size. Amer J Primatol 72(7): 575–586. doi: 10.1002/ajp.20810
- 42. Kano T (1992) The last ape: pygmy chimpanzee behavior and ecology (Stanford University Press, Stanford) 248.
- 43. Hernandez-Aguilar RA, Moore J, Stanford CB (2013) Chimpanzee nesting patterns in savanna habitat: environmental influences and preferences. Amer J Primatol 75: 979–994. doi: 10.1002/ajp.22163
- 44. Izawa K, Itani J (1966) Chimpanzees in Kasekati basin, Tanganyika: (1) Ecological study in the rainy season 1963–1964. Kyoto: Kyoto Univ. African Studies.
- 45. Ogawa H, Kanamori M, Mukeni SH (1997) The discovery of chimpanzees in the Lwazi River area, Tanzania: a new southern distribution limit. Pan Africa News 4: 1.
- 46. Ogawa H, Moore J, Kamenya S (2006) Chimpanzees in the Ntakata and Kakungu areas, Tanzania. Prim Conserv 21: 97–101. doi: 10.1896/0898-6220.127.116.11
- 47. Ogawa H, Idani G, Moore J, Pintea L, Hernandez-Aguilar A (2007) Sleeping parties and nest distribution of chimpanzees in the savanna woodland, Ugalla, Tanzania. Int J Pramatol 28(6): 1397–1412. doi: 10.1007/s10764-007-9210-0
- 48. Ndimuligo SA (2008) Assessment of chimpanzee (Pan troglodytes) population and habitat Kwitanga Forest, western Tanzania. (WiredSpace).
- 49. Ghiglieri MP (1984) The chimpanzees of the Kibale Forest (Columbia University Press, New York).