Estimates of life history parameters in a high latitude, arid-country vervet monkey population.

We present data on life history parameters from a long-term study of vervet monkeys in the Eastern Cape, South Africa. Estimates are presented of age at first conception for females and age at natal dispersal for males, along with the probability of survival to adulthood for infants born during the study, female reproductive life-span, reproductive output (including lifetime reproductive success for a subset of females), and inter-birth interval (IBI) duration. We also assess the effect of maternal age and infant survival on length of IBI. We then go on to compare life history parameters for our population with those from two East African populations in Kenya (Amboseli and Laikipia). We find there is broad consensus across the three populations, although mean infant survival was considerably lower for the two East African sites. Such comparisons must be made cautiously, however, as local ecology across the duration of the studies obviously has an impact on the estimates obtained. With this caveat in place, we consider that the concordance between values is sufficient to enable the values reported here to be used in comparative studies of primate life history, although data from habitats with higher rainfall and lower levels of seasonality are needed, and the results presented here should not be seen as canonical.

Modeling variation in the growth of wild and captive juvenile vervet monkeys in relation to diet and resource availability.

OBJECTIVES: To compare longitudinal weight gain in captive and wild juvenile vervet monkeys and conduct an empirical assessment of different mechanistic growth models. METHODS: Weights were collected from two groups of captive monkeys and two consecutive cohorts of wild monkeys until the end of the juvenile period (~800 days). The captive groups were each fed different diets, while the wild groups experienced different ecological conditions. Three different growth curve models were compared. RESULTS: By 800 days, the wild juveniles were lighter, with a slower maximum growth rate, and reached asymptote earlier than their captive counterparts. There were overall differences in weight and growth rate across the two wild cohorts. This corresponded to differences in resource availability. There was considerable overlap in growth rate and predicted adult weight of male and females in the first, but not the second, wild cohort. Maternal parity was not influential. While the von Bertalanffy curve provided the best fit to the data sets modeled together, the Logistic curve best described growth in the wild cohorts when considered separately. CONCLUSIONS: The growth curves of the two captive cohorts are likely to lie near the maximum attainable by juvenile vervets. It may be helpful to include deviations from these rates when assessing the performance of wild vervet monkeys. The comparison of wild and captive juveniles confirmed the value of comparing different growth curve models, and an appreciation that the best models may well differ for different populations. Choice of mechanistic growth model can, therefore, be empirically justified, rather than theoretically predetermined.

Network integration and limits to social inheritance in vervet monkeys.

Social networks can be adaptive for members and a recent model (Ilany and Akçay 2016 Nat. Comm.7, 12084 (doi:10.1038/ncomms12084)) has demonstrated that network structure can be maintained by a simple process of social inheritance. Here, we ask how juvenile vervet monkeys integrate into their adult grooming networks, using the model to test whether observed grooming patterns replicate network structure. Female juveniles, who are philopatric, increased their grooming effort towards adults more than males, although this was not reciprocated by the adults themselves. While more consistent maternal grooming networks, together with maternal network strength, predicted increasing similarity in the patterning of mother-daughter grooming allocations, daughters' grooming networks generally did not match closely those of their mothers. However, maternal networks themselves were not very consistent across time, thus presenting youngsters with a moving target that may be difficult to match. Observed patterns of juvenile female grooming did not replicate the adult network, for which increased association with adults not groomed by their mothers would be necessary. These results suggest that network flexibility, not stability, characterizes our groups and that juveniles are exposed to, and must learn to cope with, temporal shifts in network structure. We hypothesize that this may lead to individual variation in behavioural flexibility, which in turn may help explain why and how variation in sociability influences fitness.