Many primates exhibit behavioral flexibility which allows them to adapt to environmental change and different habitat types. The golden monkey (Cercopithecus mitis kandti) is a little-studied endangered primate subspecies endemic to the Virunga massif and the Gishwati forest in central Africa. In the Virunga massif, golden monkeys are mainly found in the bamboo forest, while in the Gishwati forest they live in mixed tropical montane forest. Here we describe and compare the diet of golden monkeys in both fragments. Over 24 consecutive months from January 2017 we used scan sampling to record feeding and ranging behavior of two Virunga groups and one Gishwati group totaling ca. 240 individuals. We also examined the phenology of bamboo and fruit trees, key seasonal food plant species for the monkeys. Golden monkeys fed on more than 100 plant species. The Virunga groups were mostly folivorous (between 72.8% and 87.16% of the diet) and fed mostly on young bamboo leaves and bamboo shoots, while 48.69% of the diet of the Gishwati group consisted of fruit from 22 different tree and shrub species. Bamboo shoots and fruit are seasonally available foods and were consumed regularly throughout the period when they were available. Despite being the smallest of the three study groups, the Gishwati group had a larger home range area (150.07 ha) compared to both Virunga groups (25.24 and 91.3 ha), likely driven by the differences in availability and distribution of fruit and bamboo in the habitats. Like other blue monkey subspecies, golden monkeys appear to have a flexible dietary strategy enabling them to adjust diet and ranging behavior to local habitats and available food resources.Additional studies and continuing conservation efforts are needed to better understand how variation in feeding and ranging ecology affects reproduction, population growth, and carrying capacity.
Habitat loss and fragmentation are major threats to primate populations globally. The Endangered golden monkey Cercopithecus mitis kandti is only found in two small forest fragments: the Virunga massif in Rwanda, Uganda and the Democratic Republic of the Congo, and the Gishwati Forest in Rwanda. Little is known about the abundance and distribution of this subspecies, or threats to its survival. During 2007–2018, we collected data along 893.7 km of line transects and 354.2 km of recce trails in Volcanoes National Park and in Gishwati–Mukura National Park to estimate golden monkey density and examine any threats. In Volcanoes National Park, golden monkeys were found almost exclusively in the bamboo zone, and in Gishwati–Mukura National Park they occurred only in the remnant tropical montane Gishwati Forest. In Volcanoes National Park, density was estimated to be 7.89 (95% CI: 3.85–16.19), 5.41 (2.64–11.08), and 5.47 (3.68–8.14) groups per km2 in 2007, 2011 and 2017–2018, respectively. This corresponds to a total of 4,331 individuals (95% CI: 2,723–5,938) in 2007, 4,487 (2,903–6,071) in 2011 and 4,626 (4,165–5,088) in 2017–2018. In Gishwati Forest, group density averaged 1.98 (95% CI: 1.27–3.16) per km2, corresponding to 172 (95% CI: 154–190) individuals in 2017–2018. Survey results from Volcanoes National Park suggest that the golden monkey population has been stable during 2007–2018. Limited habitat, illegal activities such as harvesting of bamboo and firewood, and the presence of feral dogs, threaten the golden monkey in Rwanda and require continued monitoring. The development of a conservation action plan is a priority to protect this species.
The African montane bamboo Yushania alpina provides both habitat and food for many species in the Albertine Rift region. In Volcanoes National Park (VNP), Rwanda, it is especially important as a key food resource for the Endangered mountain gorilla Gorilla beringei beringei and Endangered golden guenon Cercopithecus mitis kandti. We examined temporal and spatial variation in bamboo shoots regeneration and consumption by primates, monitored between 2013 and 2018 in 82 16-m2 plots located along transects in VNP. Our analyses revealed a decline in vegetative regeneration of bamboo in recent years, which is mirrored by a decline in bamboo shoot consumption by primates; but an increase in proportional intake. Local declines in regeneration are potentially due to high intensities of herbivory, decreased amounts of rainfall during growing seasons, and natural processes that form part of the life cycle of bamboo. Moreover, spatial variation in bamboo regeneration can be explained by elevation, as well as by stand-level variation in soil acidity, vegetation density, and the density of dead bamboo culms. We discuss the potential mechanisms underlying observed temporal and spatial variations and outline possible effects of a decline in bamboo regeneration for primates and other aspects of biodiversity in VNP.
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