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Aim Species with wide distributions spanning the African Guinean and Congolian rain forests are often composed of genetically distinct populations or cryptic species with geographic distributions that mirror the locations of the remaining forest habitats. We used phylogeographic inference and demographic model testing to evaluate diversification models in a widespread rain forest species, the African foam‐nest treefrog Chiromantis rufescens. Location Guinean and Congolian rain forests, West and Central Africa. Taxon Chiromantis rufescens. Methods We collected mitochondrial DNA (mtDNA) and single‐nucleotide polymorphism (SNP) data for 130 samples of C. rufescens. After estimating population structure and inferring species trees using coalescent methods, we tested demographic models to evaluate alternative population divergence histories that varied with respect to gene flow, population size change and periods of isolation and secondary contact. Species distribution models were used to identify the regions of climatic stability that could have served as forest refugia since the last interglacial. Results Population structure within C. rufescens resembles the major biogeographic regions of the Guinean and Congolian forests. Coalescent‐based phylogenetic analyses provide strong support for an early divergence between the western Upper Guinean forest and the remaining populations. Demographic inferences support diversification models with gene flow and population size changes even in cases where contemporary populations are currently allopatric, which provides support for forest refugia and barrier models. Species distribution models suggest that forest refugia were available for each of the populations throughout the Pleistocene. Main conclusions Considering historical demography is essential for understanding population diversification, especially in complex landscapes such as those found in the Guineo–Congolian forest. Population demographic inferences help connect the patterns of genetic variation to diversification model predictions. The diversification history of C. rufescens was shaped by a variety of processes, including vicariance from river barriers, forest fragmentation and adaptive evolution along environmental gradients.

The high predation pressure in aquatic environments is generally assumed to be the ultimate cause of terrestrial breeding in anurans (Downie 1993, Magnusson & Hero 1991, Poynton 1964, Yorke 1983). It has evolved multiple times and is presently found in most anuran families (Bogart 1981, Duellman 1992). It is often associated with higher humidity and thus lower desiccation risk in tropical forests (Duellman & Trueb 1986). Most clutches that are oviposited terrestrially are either hidden in subterranean refuges or attached more or less exposed to vegetation (Duellman & Trueb 1986, Lamotte & Lescure 1977). Exposed clutches however, face the risk of desiccation, even in rain-forest environments (Rödel pers. obs.) and are still vulnerable to predation. Such disparate groups as various arthropods (Villa 1977, 1980; Villa & Townsend 1983, Vonesh 2000), frogs (Crump 1974), snakes (Roberts 1994, Scott & Starrett 1974, Warkentin 1995) and birds (Brosset 1967), have been reported to feed on these clutches. The foam nests,which occur in at least six tropical anuran families, seem to provide better protection. Their drying surface and their more or less liquid interior offers the tadpoles an aquatic environment that is well protected against desiccation and predation (Duellman & Trueb 1986, Seymour & Loveridge 1994). In addition the bubbles of the foam facilitate oxygen diffusion within the nest and may even provide a capacious oxygen store for eggs and hatched tadpoles (Seymour & Loveridge 1994). Few predators have been reported to feed on foam nests, one of which,paradoxically, is a frog (Drewes & Altig 1996). In the Taï National Park, Ivory Coast, we discovered a quite unexpected group of predators preying on foam nests and frog clutches exposed on leaves: monkeys.