Influence of Fruit Availability on the Fission–Fusion Dynamics of Spider Monkeys (<Emphasis Type="Italic">Ateles geoffroyi</Emphasis>)

Socioecological theory proposes that the flexibility in grouping patterns afforded by fission–fusion dynamics allows animals to cope with spatiotemporal variability in food abundance. We investigate the influence of fruit tree abundance and foraging environment heterogeneity on fission–fusion dynamics in a group of spider monkeys (Ateles geoffroyi) in the Yucatan peninsula, Mexico. We collected 1300 h of behavioral data and 23 samples of biweekly ecological data from August 2009 to July 2010. We measured fission–fusion dynamics through the temporal variation in the size and composition of subgroups, the spatial dispersion within and between subgroups, and the frequency of fissions and fusions. We measured habitat-wide food abundance of preferred species, including two that differ greatly in their relative abundance: Brosimum alicastrum (a hyperabundant resource) and Ficus spp. (a not so abundant resource but often represented by large trees). We evaluated the foraging environment heterogeneity through the variance in the number of trees with fruit between species. Our results show that, although habitat-wide food abundance is important, the availability of key resources strongly influences the spider monkeys’ fission–fusion dynamics. When there was a high abundance of fruit of Brosimum, subgroups tended to be more stable, smaller, and mixed sex, and their members remained close. In contrast, when Brosimum trees with fruit were scarce, females often formed large, more fluid and dispersed subgroups. Foraging environment heterogeneity had a positive effect on within-subgroup spatial dispersion and rates of fission and fusion. The complex relationships we have uncovered suggest that the flexibility afforded by fission–fusion dynamics is an adaptation to highly variable foraging environments.     

Multiple central place foraging by spider monkeys: travel consequences of using many sleeping sites

Summary Central place foraging models assume that animals return to a single central place such as a nest, burrow, or sleeping site. Many animals, however choose between one of a limited number of central places. Such animals can be considered Multiple Central Place Foragers (MCPF), and such a strategy could reduce overall travel costs, if the forager selected a sleeping site close to current feeding areas. We examined the selection of sleeping sites (central places) by a community of spider monkeys (Ateles geoffroyi) in Santa Rosa National Park, Costa Rica in relation to the location of their feeding areas. Spider monkeys repeatedly used 11 sleeping trees, and they tended to choose the sleeping site closest to their current feeding area. A comparison of the observed travel distances with distances predicted for a MCPF strategy, a single central place strategy, and a strategy of randomly selecting sleeping sites demonstrated (1) that the MCPF strategy entailed the lowest travel costs, and (2) that the observed travel distance was best predicted by the MCPF strategy. Deviations between the observed distance travelled and the values predicted by the MCPF model increased after a feeding site had been used for several days. This appears to result from animals sampling their home range to locate new feeding sites.     

Sleeping Sites and Latrines of Spider Monkeys in Continuous and Fragmented Rainforests: Implications for Seed Dispersal and Forest Regeneration

Spider monkeys (Ateles geoffroyi) use sites composed of one or more trees for sleeping (sleeping sites and sleeping trees, respectively). Beneath these sites/trees they deposit copious amounts of dung in latrines. This behavior results in a clumped deposition pattern of seeds and nutrients that directly impacts the regeneration of tropical forests. Therefore, information on the density and spatial distribution of sleeping sites and latrines, and the characteristics (i.e., composition and structure) of sleeping trees are needed to improve our understanding of the ecological significance of spider monkeys in influencing forest composition. Moreover, since primate populations are increasingly forced to inhabit fragmented landscapes, it is important to assess if these characteristics differ between continuous and fragmented forests. We assessed this novel information from eight independent spider monkey communities in the Lacandona rainforest, Mexico: four continuous forest sites and four forest fragments. Both the density of sleeping sites and latrines did not differ between forest conditions. Latrines were uniformly distributed across sleeping sites, but the spatial distribution of sleeping sites within the areas was highly variable, being particularly clumped in forest fragments. In fact, the average inter-latrine distances were almost double in continuous forest than in fragments. Latrines were located beneath only a few tree species, and these trees were larger in diameter in continuous than fragmented forests. Because latrines may represent hotspots of seedling recruitment, our results have important ecological and conservation implications. The variation in the spatial distribution of sleeping sites across the forest indicates that spider monkeys likely create a complex seed deposition pattern in space and time. However, the use of a very few tree species for sleeping could contribute to the establishment of specific vegetation associations typical of the southeastern Mexican rainforest, such as Terminalia-Dialium, and Brosimum-Dialium.     

Tree and forest characteristics influence sleeping site choice by golden lion tamarins

Lion tamarin monkeys are among a small number of primates that repeatedly use a few tree holes for the majority of their sleeping sites. To better understand why lion tamarins rely on tree holes as sleeping sites, we compared the physical characteristics of frequently used sleeping sites, infrequently used sleeping sites, and randomly selected forest locations at multiple spatial scales. From 1990 to 2004, we recorded 5,235 occurrences of sleeping site use by 10 groups of golden lion tamarins (Leontopithecus rosalia) in Poço das Antas Reserve, Rio de Janeiro State, Brazil. Of those, 63.6% were tree holes. Bamboo accounted for an additional 17.5% of observations. Frequently used tree holes were more likely to be found in living trees and their entrances were at lower canopy heights than infrequently used tree holes. We also found that frequently used sleeping sites, in comparison to random sites, were more likely to be found on hillsides, be close to other large trees, have a lower percent of canopy cover, and have larger diameter at breast height. Topography and small‐scale variables were more accurate than were habitat‐level classifications in predicting frequently used sleeping sites. There are ample tree holes available to these lion tamarins but few preferred sites to which they return repeatedly. The lion tamarins find these preferred sites wherever they occur including in mature forest and in relics of older forest embedded in a matrix of secondary forest. Am. J. Primatol. 69:976–988, 2007. © 2007 Wiley‐Liss, Inc.     

Ecological constraints on group size in three species of neotropical primates

The foraging strategies and association patterns of 3 species of primates (Ateles geoffroyi, Alouatta palliata, Cebus capucinus) were studied over a 5-year period. The objective of the study was to provide a quantitative test of the hypothesis that the size, density and distribution of food resources influence the size of animal groups. In examining the assumptions of this hypothesis, it was shown that these primates used resources that occurred in patches, depleted the patches through their use, and that membership in large subgroups was associated with increased travel costs. The howler and spider monkey groups formed subgroups, the size of which could be predicted from the size, density and distribution of their plant food resources. When resources were clumped and at a low density, both the howler and spider monkeys were found in small subgroups, whereas when patches were uniformly distributed and at high density they formed larger subgroups. Capuchin monkeys, in contrast, did not respond to changes in these ecological variables by forming subgroups or changing the cohesion of their group.     

Sleeping site preferences in tufted capuchin monkeys (Cebus apella nigritus)

The characteristics and availability of the sleeping sites used by a group of 27 tufted capuchin monkeys (Cebus apella nigritus) were studied during 17 months at the Iguazu National Park, Argentina. We tested different hypotheses regarding possible ultimate causes of sleeping-site selection. Most sleeping sites were located in areas of tall, mature forest. Of the 34 sleeping sites the monkeys used during 203 nights, five were more frequently used than the others (more than 20 times each, constituting 67% of the nights). Four species of tree (Peltophorum dubium, Parapiptadenia rigida, Copaifera langsdorfii and Cordia trichotoma) were the most frequently used. They constituted 82% of all the trees used, though they represent only 12% of the trees within the monkeys' home range which had a diameter at breast height (DBH) > 48.16 cm (1 SD below the mean DBH of sleeping trees). The sleeping trees share a set of characteristics not found in other trees: they are tall emergent (mean height +/- SD = 31.1+/-5.2 m) with large DBH (78.5+/-30.3 cm), they have large crown diameter (14+/-5.5 m), and they have many horizontal branches and forks. Adult females usually slept with their kin and infants, while peripheral adult males sometimes slept alone in nearby trees. We reject parasite avoidance as an adaptive explanation for the pattern of sleeping site use. Our results and those from other studies suggest that predation avoidance is a predominant factor driving sleeping site preferences. The patterns of aggregation at night and the preference for trees with low probability of shedding branches suggest that social preferences and safety from falling during windy nights may also affect sleeping tree selection. The importance of other factors, such as seeking comfort and maintaining group cohesion, was not supported by our results. Other capuchin populations show different sleeping habits which can be explained by differences in forest structure and by demographic differences.     

西藏红拉雪山滇金丝猴的夜宿地与夜宿树选择

树栖灵长类动物要在夜宿地度过半生以上的时光,因此选择合适的夜宿地及夜宿树对其存活尤为关键。影响夜宿地以及夜宿树选择的主要因素是逃避天敌捕食,但对于栖息在温带森林的灵长类而言,还必须面对低 温以及食物缺乏等因素的影响。2003 年6 月至2005 年3 月,采用跟踪猴群,记录夜宿地并依据地面粪便颗粒数确定夜宿树,在西藏红拉雪山自然保护区对小昌都滇金丝猴的夜宿地及夜宿树进行了研究。结果表明:在主要 研究时间段196 d 夜宿地记录中猴群使用了101 个夜宿地,使用2 次以上的夜宿地有67 个,夜宿162 d。夜宿地全部位于针叶林中,冬季夜宿地主要分布在向阳、背风和低海拔处。比较重复利用夜宿次数多与夜宿次数少的树发现:夜宿多的树高大,底枝长,而与底枝高没有差异。比较夜宿和不过夜的树发现:夜宿树高大、底枝长。这些特点表明小昌都猴群夜宿地及夜宿树的选择可能受到逃避天敌和体温调节的影响。     

Sleeping sites, sleeping trees, and sleep-related behaviors of black crested gibbons (Nomascus concolor jingdongensis) at Mt. Wuliang, Central Yunnan, China

Data on sleep-related behaviors were collected for a group of central Yunnan black crested gibbons (Nomascus concolor jingdongensis) at Mt. Wuliang, Yunnan, China from March 2005 to April 2006. Members of the group usually formed four sleeping units (adult male and juvenile, adult female with one semi-dependent black infant, adult female with one dependent yellow infant, and subadult male) spread over different sleeping trees. Individuals or units preferred specific areas to sleep; all sleeping sites were situated in primary forest, mostly (77%) between 2,200 and 2,400 m in elevation. They tended to sleep in the tallest and thickest trees with large crowns on steep slopes and near important food patches. Factors influencing sleeping site selection were (1) tree characteristics, (2) accessibility, and (3) easy escape. Few sleeping trees were used repeatedly by the same or other members of the group. The gibbons entered the sleeping trees on average 128 min before sunset and left the sleeping trees on average 33 min after sunrise. The lag between the first and last individual entering the trees was on average 17.8 min. We suggest that sleep-related behaviors are primarily adaptations to minimize the risk of being detected by predators. Sleeping trees may be chosen to make approach and attack difficult for the predator, and to provide an easy escape route in the dark. In response to cold temperatures in a higher habitat, gibbons usually sit and huddle together during the night, and in the cold season they tend to sleep on ferns and/or orchids.     

Use of sleeping trees by black and white Colobus monkeys (Colobus guereza) in the Kakamega Forest,Kenya

Groups of black and white colobus monkeys, or guerezas (Colobus guereza), observed in the Kakamega Forest, Kenya, had weak fidelity for sleeping sites. Groups often slept in trees near commonly used food sources, which might reduce the time and energetic costs of travel. Although the home range of each group overlapped with four to seven others, groups seemed to avoid sleeping near other groups, which would give them immediate and exclusive access to nearby food sources in the morning. The number of times a species of tree was slept in was positively correlated with its density. This may have occurred because so many suitable sites were available that proximity to feeding trees could be obtained whether or not groups slept in the feeding trees. Groups slept in tall trees, which provide stable sleeping sites and which may provide protection from both aerial and ground predators. Groups were more tightly clustered on nights with greater visibility, which might reduce the risk of predation. Am. J. Primatol. 45:281–290, 1998. © 1998 Wiley-Liss, Inc.     

白马雪山自然保护区格花箐滇金丝猴夜宿地的季节性选择

2005年9月至2006年9月,在白马雪山自然保护区南端的格花箐,对一群(约250只)滇金丝猴的夜宿地选择与利用情况进行调查.整个调查历时13个月,确认研究群的夜宿点54个,共记录夜宿地的利用次数137次,提示研究群在其中一些地点多次夜宿.滇金丝猴夜宿地在平均海拔分布上存在明显的季节性差异:夏季猴群夜宿地的平均海拔为3 352 m,为一年中夜宿地分布最高的时期;春季猴群则多选择在低海拔地区夜宿,平均海拔在一年中最低(3 082 m).猴群夜宿地集中分布于3 200～3 400 m的海拔范围,随季节变化,不同海拔梯度上的夜宿地数量和利用频次差异明显.虽然猴群夜宿地主要位于针阔混交林中,但是不同季节猴群夜宿地植被的组成明显不同.猴群明显偏好在位于南坡面和西坡面的地点过夜,在夏季和秋季尚未发现北坡向的夜宿地.研究还表明,不同季节,猴群都会不同程度地在少数几个地点多次过夜,但大多数夜宿地在一年中仅利用一次.滇金丝猴为什么会对某些地点多次利用尚需进一步研究证实.     

Sleeping site selection and presleep behavior in wild pigtailed macaques

Several factors are likely to control sleeping site selection and presleep behavior in nonhuman primates, including predation risk and location of food resources. We examined the effects of these factors on the sleeping behavior of northern pigtailed macaques (Macaca leonina). While following a troop living in the surroundings of the Visitor Center of Khao Yai National Park (Thailand), we recorded the physical characteristics and location of each sleeping site, tree, the individuals' place in the tree, posture, and behavior. We collected data for 154 nights between April 2009 and November 2010. The monkeys preferred tall sleeping trees (20.9 ± SD 4.9 m) and high sleeping places (15.8 ± SD 4.3 m), which may be an antipredator strategy. The choice of sleeping trees close to the last (146.7 ± SD 167.9 m) or to the first (150.4 ± SD 113.0 m) feeding tree of the day may save energy and decrease predation risk when monkeys are searching for food. Similarly, the choice of sleeping sites close to human settlements eases the access to human food during periods of fruit scarcity. Finally, the temporal pattern of use of sleeping sites, with a preference for four of the sleeping sites but few reuses during consecutive nights, may be a trade‐off between the need to have several sleeping sites (decreasing detection by predators and travel costs to feeding sites), and the need to sleep in well‐known sites (guaranteeing a faster escape in case of predator attack). Am. J. Primatol. 73:1222–1230, 2011. © 2011 Wiley Periodicals, Inc.     

Aggregated seed dispersal by spider monkeys limits recruitment to clumped patterns in Virola calophylla

The initial spatial pattern of seed deposition influences plant population and community structure, particularly when that pattern persists through recruitment. In a vertebrate‐dispersed rain forest tree, Virola calophylla, we found that spatially aggregated seed deposition strongly influenced the spatial structure of later stages. Seed dispersion was clumped, and seed densities were highest underneath V. calophylla females and the sleeping sites of spider monkeys (Ateles paniscus), the key dispersal agent. Although these site types had the lowest per capita seed‐to‐seedling survival, they had the highest seedling/sapling densities. Conversely, seed and seedling/sapling densities were lowest, and seed survival was highest, at sites of diurnal seed dispersal by spider monkeys. Negative density‐dependent and positive distance‐dependent seed survival thinned seed clumps. Nonetheless, the clumped dispersion at sleeping and parental sites persisted to the seedling/sapling stage because differences in seed deposition were large enough to offset differences in seed survival among these site types.     

Spider Monkeys (Ateles geoffroyi yucatenensis) Cope with the Negative Consequences of Hurricanes Through Changes in Diet, Activity Budget, and Fission–Fusion Dynamics

Hurricanes can bring about dramatic changes to ecosystems and adversely affect animals that live in them. We monitored behavioral responses in wild spider monkeys (Ateles geoffroyi yucatanensis) in the aftermath of two hurricanes (Emily and Wilma) that moved through the Yucatan peninsula in 2005. We predicted that the monkeys would shift their diets depending on relative food availability and experience a change in the distribution of activity patterns. Because spider monkeys’ social organization is characterized by a high degree of fission–fusion dynamics, we predicted they would form smaller subgroups subsequent to the hurricanes to mitigate competition over limited food resources. We compared their responses in the immediate aftermath of Hurricane Emily and across the dry seasons before and after both hurricanes, to control for seasonal changes, by examining their activity budgets, foods consumed, and subgrouping dynamics. In the immediate aftermath of Hurricane Emily spider monkeys spent less time moving and more time feeding on leaves than before the hurricane and they were in smaller subgroups. In the dry season after both hurricanes the monkeys spent more time resting and less time moving than before the hurricanes, and leaves replaced fruit as their primary food resource. They fused into larger subgroups less often and had smaller subgroup sizes in the dry season after than before the hurricanes. Thus, the high degree of fission–fusion dynamics of spider monkeys was instrumental in affording the behavioral flexibility critical to cope with the negative post-hurricane consequences.     

Sleeping sites and lodge trees of the night monkey (Aotus azarae) in Bolivia

Between 1984 and 1987, we recorded the sleeping-site and lodge tree preferences of night monkeys at the Beni Biological Station, Bolivia. We characterized the structure of sleeping-site compared lodge trees to nonlodge trees, and determined the frequency of their use. Aotus azarae used branch and liana platforms on trees of the middle strate of the forest as sleeping sites, but the lodge trees provided sparse cover. Monkeys may manipulate either natural accumulations of material or bird nests to serve as sleeping sites. The characteristics of the sleeping site and of the lodge trees may be related to protection against predators and to thermal advantages. The distribution of lodge trees appeared to be related to access to food. Activities around the sleeping site could be related to marking behavior.     

Which senses play a role in nonhuman primate food selection? A comparison between squirrel monkeys and spider monkeys

In order to optimize foraging efficiency and avoid toxicosis, animals must be able to detect, discriminate, and learn about the predictive signals of potential food. Primates are typically regarded as animals that rely mainly on their highly developed visual systems, and little is known about the role that the other senses may play in food selection. It was therefore the aim of the present study to assess which senses are involved in the evaluation of food by two species of New World primates: the squirrel monkey and the spider monkey. To this end, six animals per species were repeatedly presented with both familiar and novel food items, and their behavior was videotaped and analyzed. To obtain a further indication of the relative importance of visual and chemosensory cues, the animals were also presented with familiar food items that were experimentally modified in color, odor, or both color and odor. The results demonstrate that squirrel monkeys and spider monkeys use olfactory, gustatory, and tactile cues in addition to visual information to evaluate novel food, whereas they mainly inspect familiar food items visually prior to consumption. Our findings also show that in both species the use of nonvisual cues decreased rapidly with repeated presentations of novel food, suggesting a fast multimodal learning process. Further, the two species clearly differ in their relative use of nonvisual cues when evaluating novel or modified food, with spider monkeys relying more on olfactory cues than squirrel monkeys, and squirrel monkeys relying more on tactile cues compared to spider monkeys.     

Use of sleeping trees by ursine colobus monkeys (Colobus vellerosus) demonstrates the importance of nearby food

Examination of the characteristics and locations of sleeping sites helps to document the social and ecological pressures acting on animals. We investigated sleeping tree choice for four groups of Colobus vellerosus, an arboreal folivore, on 298 nights at the Boabeng-Fiema Monkey Sanctuary, Ghana using five non-mutually exclusive hypotheses: predation avoidance, access to food, range and resource defense, thermoregulation, and a null hypothesis of random selection. C. vellerosus utilized 31 tree species as sleeping sites and the species used differed per group depending on their availability. Groups used multiple sleeping sites and minimized their travel costs by selecting trees near feeding areas. The percentage that a food species was fed upon annually was correlated with the use of that species as a sleeping tree. Ninety percent of the sleeping trees were in a phenophase with colobus food items. Entire groups slept in non-food trees on only one night. These data strongly support the access to food hypothesis. Range and resource defense was also important to sleeping site choice. Groups slept in exclusively used areas of their home range more often than expected, but when other groups were spotted on the edge of the core area, focal groups approached the intruders, behaved aggressively, and slept close to them, seemingly to prevent an incursion into their core range. However, by sleeping high in the canopy, in large, emergent trees with dense foliage, positioning themselves away from the main trunk on medium-sized branches, and by showing low rates of site reuse, C. vellerosus also appeared to be avoiding predation in their sleeping site choices. Groups left their sleep sites later after cooler nights but did not show behavioral thermoregulation, such as huddling. This study suggests that access to food, range and resource defense, and predation avoidance were more important considerations in sleeping site selection than thermoregulation for ursine colobus.     

Sleeping Site Selection by the Golden-handed Tamarin Saguinus midas midas: The Role of Predation Risk, Proximity to Feeding Sites, and Territorial Defence

Tamarin monkeys, of the genus Saguinus , spend over half their lives at arboreal sleeping sites. The decision as to which site to use is likely to have considerable fitness consequences. These decisions about sleeping sites by three troops of golden-handed tamarin Saguinus midas midas were examined over a 9-mo period at a rainforest site in French Guiana. Data are presented on the physical nature of sleeping sites, their number, position within home ranges, and pattern of use and reuse, aspects of behaviour at retirement and egress, and predation attempts on the study troops. Cumulative plot analysis indicated that a tamarin troop used 30–40 sleeping sites in a 100-day period, approximately half of which were used very infrequently, so that consecutive reuse was never greater than three nights. Sleeping trees were superior in architectural parameters and liana weight to non-sleeping trees. There were no more sleeping sites than expected within the home range boundary region of the tamarins or in areas of overlap with the home ranges of neighbouring troops. Tamarins selected sleeping sites nearest to the last feeding site of the day on 25% of occasions. The study troops engaged in a number of activities that may reduce predation risk; raptor attacks on the study troops over 9 mo were frequent but unsuccessful. Tamarins often visited a sleeping site several hours before arrival, and were more likely to visit a site before use if they had not used it recently. The decision to select a sleeping site therefore involved knowledge of the previous frequency of use of that site.     

Diets of some French guianan primates: Food composition and food choices

We studied food choices of black spider monkeys (Ateles paniscus) and red howlers (Alouatta seniculus) in an undisturbed tropical forest of French Guiana for 6 months in the rainy season. We made additional observations on tufted capuchins (Cebus apella) and examined the differences and similarities in feeding behavior with respect to the plant specific composition of the habitat and the biochemical characteristics of their food. Capuchins and spider monkeys mainly fed on ripe fruit pulp, to which they added invertebrates (capuchins) or young leaves (spider monkeys); their plant diet was more varied than that of howlers, which contained approximately equal proportions of ripe fruits and young leaves of many species, with large monthly variations in these food categories. BothAteles andAlouatta tended to feed preferentially on abundant plant species, with a large overlap in their fruit choices. The former species included a high proportion of soluble sugars and a low proportion of protein in its diet compared, to howlers. Leaves of several species selected byAlouatta reacted positively when screened for alkaloids and phenolic compounds. Besides specific metabolic requirements and adaptations to deriving nutrients from distinct food types, we hypothesize that the ability to taste sugars, which varies among primates, affects the range of foods appearing to be palatable and, consequently, contributes to the differentiation of feeding niches.     

Multiple Ecological Factors Influence the Location of Proboscis Monkey (<Emphasis Type="Italic">Nasalis larvatus</Emphasis>) Sleeping Sites in West Kalimantan,Indonesia

Multiple ecological factors have been hypothesized to influence primate sleeping site selection. Testing multiple hypotheses about sleeping site selection permits examination of the relative strength of distinct ecological factors and expands our ability to understand how selection pressures influence primate sleeping behavior. Here we examine how avoidance of biting insects, thermoregulation, foraging efficiency, tree stability, and interspecific competition influence selection of sleeping sites by proboscis monkeys (Nasalis larvatus) in Indonesian Borneo. We collected data on relative insect abundance, temperature, rainfall, food availability, group size, sleeping site location, and presence of other primates for 12 mo. Using formal model comparison and information criteria, we analyzed the relative importance of these ecological factors in determining one aspect of sleeping site location: distance from the river. Our models supported the avoidance of biting insects and the foraging efficiency hypotheses. Proboscis monkeys slept further inland on nights when the abundance of sandflies was high along the river, and when less food was available along the river. Many studies suggest that primates select sleeping trees and locations to reduce predation risk; our study indicates that additional factors may also be important in determining sleeping site selection.     

Sleeping Sites of <Emphasis Type="Italic">Rhinopithecus brelichi</Emphasis> at Yangaoping,Guizhou

Arboreal primates spend about half of their lives at sleeping sites; hence, selection of sleeping sites is crucial for individual survival, and data concerning them is important for conservation efforts. We collected data on sleeping sites for a group of the endangered snub-nosed monkey (Rhinopithecus brelichi) at Yangaoping (27°58′N, 108°45′E) from January 2006 to December 2007. All sleeping sites were located in the mid-slope and in the shadow of ridges facing the northeast and southeast. The monkeys remained quiet while entering and occupying sleeping sites, and slept in evergreen species during the cold season (December–March). Trees in sleeping sites were similar in height and girth at breast height to those elsewhere, but some trees in lower areas were larger. The monkeys usually slept in close proximity to the last feeding spot, and their daily activities usually occurred around the sleeping site. Areas adjacent to sleeping sites were used more intensively than those not adjacent. Monkeys left the sleeping sites later in the morning in the cold season. These behavioral responses suggested that predation risk, thermoregulation, and climate stresses are the main determining factors in the selection of sleeping sites for this temperate monkey.