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Demos, T. C.

Publications and source records attributed to Demos, T. C..

2 recordsLinked to original sources

Incipient speciation, rapid expansion and repeated introgressive hybridization in an African Giant Shrew (Crocidura olivieri)

The African giant shrew (Crocidura olivieri) is one of the most widespread native small mammals in sub-Saharan Africa, occupying habitats ranging from humid tropical forests to arid Savanna. Its broad distribution, ecological diversity, and unresolved evolutionary relationships suggest a history of rapid diversification, yet the roles of hybridization and demographic expansion remain poorly understood. We combined genome-wide ddRAD and mitochondrial data from populations sampled across sub-Saharan Africa to reconstruct the evolutionary history of African giant shrews. We reveal extensive mitonuclear discordance across the clade and show that it reflects a complex history of repeated introgressive hybridization rather than a single evolutionary event. Genomic analyses resolve three major evolutionary lineages and identify four introgression events, including extensive bidirectional genome-wide introgression between the ancestors of the C. olivieri and arid adapted species followed by later unidirectional introgression associated with range expansion. Within the C. olivieri group, we identify five geographically structured lineages connected by ongoing gene flow, representing different stages of incipient speciation. Demographic analyses further reveal repeated population expansion during the Late Pleistocene and Early Holocene, with lineage-specific timing consistent with climatic fluctuations and a possible contribution of increasing human association. Our results identify repeated range expansion and hybridization as major drivers of diversification in African giant shrews and establish this system as a powerful model for studying the genomic processes underlying early speciation.

evolutionary biology↗

Associations between Afrotropical bats, parasites, and microbial symbionts

Bats are among the most diverse animals on the planet and harbor numerous bacterial, viral, and eukaryotic symbionts. The interplay between bacterial community composition and parasitism in bats is not well understood and may have important implications for studies of similar systems. Here we present a comprehensive survey of dipteran and haemosporidian parasites, and characterize the gut, oral, and skin microbiota of Afrotropical bats. We identify significant correlations between bacterial community composition of the skin and dipteran ectoparasite prevalence across four major bat lineages, as well as links between the oral microbiome and malarial parasitism, suggesting a potential mechanism for host selection and vector-borne disease transmission in bats. In contrast to recent studies of host-microbe phylosymbiosis in mammals, we find no correlation between chiropteran phylogenetic distances and bacterial community dissimilarity across the three anatomical sites, suggesting that host environment is more important than shared ancestry in shaping the composition of bat-associated bacterial communities.\n\nSIGNIFICANCEAnimals rely on bacterial symbionts for numerous biological functions, such as digestion and immune system development. Increasing evidence suggests that host-associated microbes may play a role in mediating parasite burden. This study is the first to provide a comprehensive survey of bacterial symbionts from multiple anatomical sites across a broad taxonomic range of Afrotropical bats, demonstrating significant associations between the bat microbiome and parasite prevalence. This study provides a framework for future approaches to systems biology of host-symbiont interactions across broad taxonomic scales, emphasizing the interdependence between microbial symbionts and vertebrate health in the study of wild organisms and their natural history.

ecology↗