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The identification of seed dispersers and predators is essential to understand the effect of anthropogenic disturbances, and the associated defaunation process, on tropical forest dynamics in Central Africa. In this study, the animals involved in seed predation and dispersal of Dacryodes normandii (Burseraceae), an endozoochorously dispersed tree species endemic to Gabonese forests, were identified in a site in south-east Gabon using two complementary methods: direct observation and camera-trap monitoring of fruit piles. The combined sampling effort (172 h of direct observations and 796 d of camera trapping) led to the identification of six disperser and eight predator species of D. normandii seeds. With high frequency of consumption (88% and 57% of their visits, respectively) and long visit duration (83 and 23 min, respectively), the western lowland gorilla and central chimpanzee were identified as the main dispersers of this species. Seeds passed through the gorilla gut exhibited high germination success (68%). Rodents were identified as predators of D. normandii seeds, potentially displaying rare secondary dispersal through scatter-hoarding. The results of this study highlight the importance of great apes in the seed dispersal of this tree species.
Understanding the ecological function of large frugivores in tropical forests is important considering their central position in seed-dispersal networks. This study illustrates the seed-dispersal effectiveness of a western lowland gorilla (Gorilla gorilla gorilla) population in Cameroon by looking at the interaction of seed quantity, species regeneration traits and the environmental characteristics of the deposition sites (sleeping sites vs. feeding trails) in order to discuss the role of gorillas within the ecosystem. The analysis of 1030 faecal samples collected over a 3-y period (September 2009–August 2012) showed that gorillas dispersed a diverse array of species (58 spp. identified), with an average of 289 intact seeds (>5 mm) d−1 per individual. Seed damage during mouth and gut processing occurred for 12 spp., generally accounting for <5% of specific seed load. Germination trials suggested that germination success of passed seeds remained unchanged (N = 6 spp.) or improved (N = 5 spp.) after gut passage compared with hand-cleaned seeds, with one exception. Indicator species identification (IndVal method) and General Discriminant Analysis suggested that sleeping sites (N = 36), as a main type of seed deposition site, correspond to regenerating microhabitats and correspondingly degree of canopy openness is one variable discriminating significantly this type of deposition site with random locations in the forest (N = 36) used as a proxy for non-directed seed deposition on feeding trails. With a mean canopy openness of 19–27%, sleeping sites offer optimal light conditions for the seedling recruitment of non-pioneer light-demanding species, the seeds of which encompass 47.4% of the total seed load dispersed over the 3-y period. From this study, it is hypothesized that the gorilla performed directed-dispersal of some light-demanding plant species at sleeping sites, and hence, by being actively implicated in gap-phase dynamics, fulfils a valuable ecological function within its ecosystem.
For endozoochorous seed dispersal systems, the extant dung beetle assemblage at seed deposition sites may influence site suitability as burial activity may change the probability that seeds germinate and seedlings establish. This study tested if the different conditions of the two main seed-deposition habitats of a western lowland gorilla population of south-east Cameroon (sleeping sites and old secondary forest) influenced dung beetle assemblages and consequently the seed relocation patterns. In March 2012, in both habitats, burial patterns (proportion and depth) were described in eight stations based on two 300-g experimental faeces with known number of Uapaca spp. seeds (N = 75) left for 48 h, and beetle assemblages were described based on one 48h-dung-baited pitfall trapping session in five of these stations. To assess the impact of burial pattern on seedling emergence, Uapaca seedling emergence trials were performed in a nursery (75 seeds per depth treatment). Assemblage at sleeping sites had a higher species richness (non-significant) and was significantly more abundant than in old secondary forests. Conversely, significantly more seeds were buried in old secondary forests than sleeping sites and at significantly greater depths (mean: 14.9 cm vs. 8.7 cm). As trials suggested that burial depth ≥7 cm prevented Uapaca seedling emergence, dung beetles are assumed to induce seed loss more strongly in old secondary forests than sleeping sites (20.5% vs. 6.7% of initial seed crop). The demonstration that dung beetles may exert a negative influence on seed fate overall, and that the degree to which this occurs may vary depending on habitat, highlights the complexity in determining the suitability of deposition sites for recruitment.
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