Although dominant African wild dogs (Lycaon pictus) are generally believed to be the sole breeders within a pack, earlier behavioral and endocrine data suggest that reproduction could be shared with subordinates. We performed an extensive behavioral, demographic, and genetic evaluation of a wild dog population in South Africa to examine the level of such sharing and the proximate mechanisms influencing reproductive contributions of each sex. While a majority of pups were born to dominants because of a lack of subordinate potential breeders, we discovered a substantial portion of reproductive sharing between dominants and subordinates. Compared with alpha females that mated annually, subordinate beta females bred in 54.5% of years whereas thetas never bred. The three topranking males all sired pups (56.0%, 32.0%, and 12.0%, respectively) when three or more adult males were present. With only two pack males, alpha and beta individuals shared reproduction nearly equally (55.2% and 44.8%, respectively), and litters of mixed paternity were discovered on eight of 15 (53.3%) occasions. A skewed adult sex-ratio and frequent alpha mortalities for females and behavioral aggression in males allowed most individuals to attain dominant status in their lifetime, creating a constantly shifting social hierarchy. Genetic parentage results corresponded to reported hormone profiles, suggesting physiological suppression in some lower-ranked individuals of both sexes. Thus, a combination of demographic, behavioral, and hormonal proximate factors mediates reproductive partitioning in wild dogs. We conclude that reproductive sharing can be significant in this species, especially for males that have less robust suppressive mechanisms than females.
It is crucial to understand the genetic health and implications of inbreeding in wildlife populations, especially of vulnerable species. Using extensive demographic and genetic data, we investigated the relationships among pedigree inbreeding coefficients, metrics of molecular heterozygosity and fitness for a large population of endangered African wild dogs (Lycaon pictus) in South Africa. Molecular metrics based on 19 microsatellite loci were significantly, but modestly correlated to inbreeding coefficients in this population. Inbred wild dogs with inbreeding coefficients of C0.25 and subordinate individuals had shorter lifespans than outbred and dominant contemporaries, suggesting some deleterious effects of inbreeding. However, this trend was confounded by packspecific effects as many inbred individuals originated from a single large pack. Despite wild dogs being endangered and existing in small populations, findings within our sample population indicated that molecular metrics were not robust predictors in models of fitness based on breeding pack formation, dominance, reproductive success or lifespan of individuals. Nonetheless, our approach has generated a vital database for future comparative studies to examine these relationships over longer periods of time. Such detailed assessments are essential given knowledge that wild canids can be highly vulnerable to inbreeding effects over a few short generations.
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