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. 2025 Jul 31;15(8):e71879.
doi: 10.1002/ece3.71879. eCollection 2025 Aug.

Incipient Genetic Differentiation of the African Buffalo, Syncerus caffer Populations: Is Fencing Playing a Role?

Affiliations

Incipient Genetic Differentiation of the African Buffalo, Syncerus caffer Populations: Is Fencing Playing a Role?

Patrick Karanja et al. Ecol Evol. .

Abstract

Fences are increasingly used globally as a management tool in conservation to reduce wildlife depredations, disease transmission, and wildlife mortality. There are a limited number of studies on the genetic effects of perimeter fencing of protected areas on megaherbivores. Using population genetic analyses on 226 sequences of a 400 bp fragment of the mtDNA Dloop from 10 East African buffalo populations (3 fenced and 7 unfenced), the influence of spatial isolation and fencing on buffalo population genetic diversity and genetic differentiation was examined. Mean gene diversity between fenced and unfenced buffalo populations was not different (fenced: 0.978 ± 0.003, unfenced: 0.973 ± 0.004, p = 0.300), but nucleotide diversity was higher in fenced than unfenced populations (fenced: 0.038 ± 0.019, unfenced: 0.030 ± 0.015, p = 0.005). Genetic differentiation among buffalo populations based on haplotype frequencies and model-based genetic distance was weak (FST = 0.08, ΦST = 0.06) and contributed to 6.2% and 8.5% of total genetic variance, respectively. Ninety-three percent of population pairs were genetically differentiated by distances determined from haplotype frequencies, but only 51% of population pairs were differentiated using modeled distances, suggesting recent differentiation. There was no correlation between linearized FST and geographical distance (r = -0.005, p = 0.52), but linearized ΦST was moderately correlated with geographic distance (r = 0.329, p = 0.03). The distance effect was greater when fenced populations were excluded (ΦST: r = 0.464, p = 0.05), suggesting that insularization due to fencing is distorting isolation by distance. SSD analyses revealed that 2 of 3 fenced populations and 2 of 7 unfenced populations had non-unimodal distributions, suggesting demographically declining populations. Our study reveals the high genetic diversity but warns that genetic erosion due to isolation, including fencing, is likely setting in and will have an impact on East African buffalo populations.

Keywords: African ungulates; D‐loop; conservation; fencing; mtDNA; protected areas.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Map showing locations of the study buffalo populations in Kenya and Tanzania. Mpala Wildlife Conservancy (MPWC), Ol Jogi Wildlife Conservancy (OJWC), Maswa Game Reserve (MSGR), Ngorongoro Conservation Area (NGCA), Serengeti National Park (SENP) and Maasai Mara National Reserve (MMNR), Masaai Mara National Reserve (MMNR), Lake Nakuru National Park (LNNP), Ol Pejeta Wildlife Conservancy (OPWC), Tsavo East National Park (TENP) and Solio Wildlife Conservancy (SOWC).
FIGURE 2
FIGURE 2
The distribution of haplotype copies (A) and haplotype sharing between the African Buffalo populations (B) in Kenya and Tanzania.
FIGURE 3
FIGURE 3
Minimum spanning haplotype network showing relationships among haplotypes in 10 buffalo populations in East Africa.
FIGURE 4
FIGURE 4
Correlations between genetic distance and spatial distance between buffalo populations in East Africa. (A) Genetic distance was determined using the HKY + G + I nucleotide substitution model on all populations (r = 0.329, p = 0.0298) and (B) excluding fenced populations (r = 0.464, p = 0.0499). In (C) genetic distance is determine from haplotype frequencies for all populations (r = −0.00451, p = 0.518) and (D) excluding fenced populations (r = 0.0269, p = 0.458).
FIGURE 5
FIGURE 5
Mismatch distributions showing observed nucleotide differences (histogram) and expected differences from a population expansion model (line graph) for several buffalo populations.

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