| Literature DB >> 23878333 |
K A Abernethy1, L Coad, G Taylor, M E Lee, F Maisels.
Abstract
Humans have hunted wildlife in Central Africa for millennia. Today, however, many species are being rapidly extirpated and sanctuaries for wildlife are dwindling. Almost all Central Africa's forests are now accessible to hunters. Drastic declines of large mammals have been caused in the past 20 years by the commercial trade for meat or ivory. We review a growing body of empirical data which shows that trophic webs are significantly disrupted in the region, with knock-on effects for other ecological functions, including seed dispersal and forest regeneration. Plausible scenarios for land-use change indicate that increasing extraction pressure on Central African forests is likely to usher in new worker populations and to intensify the hunting impacts and trophic cascade disruption already in progress, unless serious efforts are made for hunting regulation. The profound ecological changes initiated by hunting will not mitigate and may even exacerbate the predicted effects of climate change for the region. We hypothesize that, in the near future, the trophic changes brought about by hunting will have a larger and more rapid impact on Central African rainforest structure and function than the direct impacts of climate change on the vegetation. Immediate hunting regulation is vital for the survival of the Central African rainforest ecosystem.Entities:
Keywords: Central Africa; ecological function; future; hunting; land-use change; wildlife
Mesh:
Year: 2013 PMID: 23878333 PMCID: PMC3720024 DOI: 10.1098/rstb.2012.0303
Source DB: PubMed Journal: Philos Trans R Soc Lond B Biol Sci ISSN: 0962-8436 Impact factor: 6.237
Village and commercial hunting distances.
| ( | |||
|---|---|---|---|
| source | site | method | maximum distance of traps and hunting camps from village |
| [ | Ekom, Cameroon | GPS follow | hunting camps: 18 km |
| [ | Oleme and Diba, ROC | GPS follow | traplines: 8.0 (Oleme) and 3.9 km (Diba) |
| [ | Ituri, DRC | estimate | most hunting occurs within approximately 15 km of settlements |
| [ | Mossapouna, CAR | GPS follow | day hunting: 10 km from village; hunting camps: 21 km from village |
| [ | Sendje, Equatorial Guinea | GPS follow | hunting camps: 30 km, hunters trap a max of 3.2 km from the village or a hunting camp (1 day trip) |
| [ | Zoulabot Ancien, Cameroon | GPS follow | hunting camps: 21.5 km from village, snares set in a radius of approximately 3 km from camp; every 2 years hunters stay in a hunting camp less than 50 km from the village, for 2 months or more |
| [ | Mekas, Cameroon | estimate | village hunting: approximately 5–10 km; hunting camps: approximately 40 km |
| [ | Nsiete, Gabon | hunter interviews | more than 10 km in the dry season. Less than 2 km in the wet season |
| [ | Midyobo Anvom, Equatorial Guinea | GPS follow | hunting camps: 13.2 km, hunters travelled 2–3 km from hunting camps to place traps |
| [ | Dibouka and Kouagna, Gabon | GPS follow | village traplines: 6.5 km; hunting camps 12.7 km |
| ( | |||
| source | site | furthest record of hunting sign, from nearest road or river (foot transect surveys; in kilometres) | |
| [ | Nouabale Ndoki, protected landscape ROC | <20 | |
| [ | Ntokou Pikounda forest, ROC | <25 | |
| [ | Mbam Djerem National Park, Cameroon | <27 | |
| [ | Odzala-Koukoua National Park, ROC | <30 | |
| [ | Sankuru landscape, DRC | <40 | |
| [ | Lopé National Park, Gabon | <22 | |
| [ | Mont de Cristal, Gabon | <10 | |
| [ | Lac Tele National Park, ROC | <25 | |
| [ | Waka National Park, Gabon | <10 | |
aMaximum trapping distances calculated for this paper; analysis of trapping distances and methods can be found in Coad et al. [31].
Figure 1.The impact of village hunting on trophic guilds of the Central African forests. Classification of species to these guilds can be found in the electronic supplementary material, table S1. Grey bars represent non-seed disperser, and black bars represent seed disperser.
Empirical evidence of the impacts of hunting on ecological function in tropical forest ecosystems.
| disruption to ecological functioning as a result of hunting | examples from literature | empirical studies from African rainforests | empirical studies from other tropical forests | |
|---|---|---|---|---|
| changes in wildlife assemblages | interspecific competition (between predator and prey) | apex and mesopredators inhabiting heavily hunted areas are forced to prey on smaller species through direct competition with hunters for larger bodied species; this reduces predator population sizes | [ | [ |
| interspecific competition (between prey species) | heavy hunting pressure and selective hunting can change the competitive balance between sympatric species; many species have separate niches due to competition rather than habitat constraints | [ | [ | |
| ecological and predator release | as large herbivores and top predators are extirpated, an initial increase in secondary game species is witnessed; populations of small, non-target species increase but overall animal biomass decreases | [ | [ | |
| changes in relative seed dispersal success | seed dispersal failure due to seed predators both increasing and switching to more abundant seeds | in heavily hunted areas, rodents and other small seed predators switch feeding behaviour to animal-dispersed species whose undispersed seeds are now found in clusters around the parent plant | [ | [ |
| reduced seed dispersal, sapling recruitment and plant regeneration | in hunted areas where large, long distance dispersers are absent, rates of dispersal and regeneration of animal-dispersed trees are much lower than where these species are present | [ | [ | |
| increased kin competition between seedlings | seedlings, which remain under parent plant due to reduced dispersal in hunted areas, experience increased competition | [ | ||
| changes in relative pre-dispersion predation pressure for seeds | pre-dispersal seed predation by larger mammals is higher in protected areas than in hunted areas | [ | ||
| changes in vegetation structure and composition | reduced plant species richness and diversity | tree species richness is lower in regenerating cohorts in hunted areas than in protected sites | [ | [ |
| changes in tree spatial structure | increased clustering and densities of saplings of animal-dispersed plants due to loss of large herbivores | [ | [ | |
| increased proportion of lianas (and other wind-dispersed species) due to decrease in animal seed dispersers | wind-dispersed climbing species, which are overwhelmingly woody lianas, are found in higher proportions in the seedling bank at heavily hunted sites than at protected sites | [ | [ | |
| changes in vegetation composition | diversity of plants with large- and medium-sized seeds was significantly lower while diversity of plants with small-sized seeds increased significantly with hunting pressure | [ | [ | |
| soil quality | altered nutrient cycling and parasite suppression, disturbed soil fertilization and aeration | reduced abundance of Scarabaeinae beetles as a result of reduced availability of mammal dung alters ecosystem functioning | [ | |
| carbon balance | reduced carbon storage | reduced woody plant recruitment due to decreased large seed species will threaten carbon-storage capacity | [ |