12 research outputs found

    Demography and Life Histories of Sympatric Patas Monkeys, Erythrocebus patas, and Vervets, Cercopithecus aethiops, in Laikipia, Kenya

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    Mortality patterns are thought to be strong selective forces on life history traits, with high adult mortality and low immature mortality favoring early and rapid reproduction. Patas monkeys (Erythrocebus patas) have the highest potential rates of population increase for their body size of any haplorhine primate because they reproduce both earlier and more often. We report here 10 yr of comparative demographic data on a population of patas monkeys and a sympatric population of vervet monkeys (Cercopithecus aethiops), a closely related species differing in aspects of social system, ecology, and life history. The data reveal that 1) adult female patas monkeys have significantly higher mortality than adult female vervets; 2) infant mortality in patas monkeys is relatively low compared to the norm for mammals because it is not significantly different from that of adult female patas monkeys; and 3) infant mortality is significantly higher than adult female mortality in vervets. For both species, much of the mortality could be attributed to predation. An epidemic illness was also a major contributor to the mortality of adult female patas monkeys whereas chronic exposure to pathogens in a cold and damp microenvironment may have contributed to the mortality of infant vervets. Both populations experienced large fluctuations during the study period. Our results support the prediction from demographic models of life history evolution that high adult mortality relative to immature mortality selects for early maturation

    Effects of Habitat Structure on Perceived Risk of Predation and Anti-Predator Behavior of Vervet (Cercopithecus aethiops) and Patas (Erythrocebus patas) Monkeys

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    Reproductive seasonality in primates: patterns, concepts and unsolved questions

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    Primates, like other mammals, exhibit an annual reproductive pattern that ranges from strictly seasonal breeding to giving birth in all months of the year, but factors mediating this variation are not fully understood. We applied both a categorical description and quantitative measures of the birth peak breadth based on daily observations in zoos to characterise reproductive seasonality in 141 primate species with an average of 941 birth events per species. Absolute day length at the beginning of the mating season in seasonally reproducing species was not correlated between populations from natural habitats and zoos. The mid‐point of latitudinal range was a major factor associated with reproductive seasonality, indicating a correlation with photoperiod. Gestation length, annual mean temperature, natural diet and Malagasy origin were other important factors associated with reproductive seasonality. Birth seasons were shorter with increasing latitude of geographical origin, corresponding to the decreasing length of the favourable season. Species with longer gestation periods were less seasonal than species with shorter ones, possibly because shorter gestation periods more easily facilitate the synchronisation of reproductive activity with annual cycles. Habitat conditions with higher mean annual temperature were also linked to less‐seasonal reproduction, independently of the latitude effect. Species with a high percentage of leaves in their natural diet were generally non‐seasonal, potentially because the availability of mature leaves is comparatively independent of seasons. Malagasy primates were more seasonal in their births than species from other regions. This might be due to the low resting metabolism of Malagasy primates, the comparatively high degree of temporal predictability of Malagasy ecosystems, or historical constraints peculiar to Malagasy primates. Latitudinal range showed a weaker but also significant association with reproductive seasonality. Amongst species with seasonal reproduction in their natural habitats, smaller primate species were more likely than larger species to shift to non‐seasonal breeding in captivity. The percentage of species that changed their breeding pattern in zoos was higher in primates (30%) than in previous studies on Carnivora and Ruminantia (13 and 10%, respectively), reflecting a higher concentration of primate species in the tropics. When comparing only species that showed seasonal reproduction in natural habitats at absolute latitudes ≤11.75°, primates did not differ significantly from these two other taxa in the proportion of species that changed to a less‐seasonal pattern in zoos. However, in this latitude range, natural populations of primates and Carnivora had a significantly higher proportion of seasonally reproducing species than Ruminantia, suggesting that in spite of their generally more flexible diets, both primates and Carnivora are more exposed to resource fluctuation than ruminants

    Ranging of Rhinopithecus bieti in the Samage Forest, China. II. Use of land cover types and altitudes

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    We investigated composition and structure of a temperate montane forest called Samage at Baimaxueshan National Nature Reserve in Yunnan, one of the last refuges for the highly endangered black-and-white snub-nosed monkeys (Rhinopithecus bieti). There is a patchwork of vegetation types at Samage, and we distinguished 6 major land cover types within the home range of the focal group. We tracked the semihabituated Gehuaqing band for a full annual cycle to study their habitat utilization and altitudinal ranging. We analyzed the group’s selective use of particular habitat types via selection ratios. We calculated habitat availability from a GIS database. We found that they used mixed deciduous broadleaf/conifer forest disproportionately to its availability in all months. Subjects completely avoided meadows. Pine and evergreen broadleaf forests acted as corridors between patches of mixed forest and monkeys visited them occasionally, but at low frequencies and mostly in transit. The focal band stayed at elevations ranging from ca. 2600 m to 4000 m, and the mean elevation usedis 3200 m. We found evidence for seasonal variation in use of elevational zones. The band stayed at significantly higher elevations in summer than in spring. The descent in spring was likely related to a flush of immature leaves at low-lying elevations. Availability of preferred fruits also had a highly positive influence on altitudinal ranging, i.e., during months with high fruit availability (late summer, early fall), the band stayed at medium elevations where preferred fruits were most abundant. Higher concentrations of lichens and the snub-nosed monkeys’ search for not yet depleted fruits probably caused them to remain at mid-elevations in winter. There is no significant correlation between climate parameters and elevation used. One of the main inferences of this investigation is that, contrary to previous accounts, Rhinopithecus bieti is not universally associated with high-elevation dark fir forest, but at Samage exhibits an overwhelming preference for mixed forest. Moreover, our analyses support the hypothesis that elevational migration, in this temperate-subtropical forest, is influenced by the temporal fruiting of major food trees and that climate has only a negligible effect on elevation use

    Ranging of Rhinopithecus bieti in the Samage Forest, China. I. Characteristics of range use

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    We quantified the home range and explored the style of ranging of black-and-white snub-nosed monkeys (Rhinopithecus bieti) in the subtropical-temperate montane Samage Forest (part of Baimaxueshan Nature Reserve) in the vicinity of Gehuaqing. Over 14.5 mo, we took positional records of the study band via a GPS receiver at 30-min intervals, and found that they covered an area of 32 km2. Over a 10-yr period, the group even ranged in an area of 56 km2, which is among the largest home range estimates for any primate. The large home range was probably due to the combined effects of large group size (N > 400) and forest heterogeneity, with seasonally food-rich areas interspersed with less valuable areas. The subjects did not use their home range uniformly: 29% of the grid cells had more location records than expected based on a uniform distribution, thus representing a core area, albeit a disjunct one. A continuous 1-mo group follow in the fall revealed that the band traveled on average 1.62 km/d and that days of concentrated use of a particular forest block were followed by more extensive marches. Neither climate nor human disturbance parameters correlate significantly with monthly estimates of the group’s home range size. Even though there is no significant correlation between temporal availability of plant phenophases and range size, our observations implicate temporal and spatial availability of food as a determinant of home range use of the focal group. Winter,spring, and summer home ranges are equally large: 18.2, 17.8, and 18.6 km, respectively. Home range decreased markedly in fall (9.3 km2), probably because the band obtained sufficient food resources (fruit) in a smaller area. The large winter range is best attributed to the exploitation of dispersed clumped patches of mature fruits
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