BackgroundAnthropogenic habitat disturbance is a prime cause in the current trend of the Earth’s reduction in biodiversity. Here we show that the human footprint on the Central African rainforest, which is resulting in deforestation and growth of densely populated urban agglomerates, is associated to ecological divergence and cryptic speciation leading to adaptive radiation within the major malaria mosquito Anopheles gambiae.Methodology/Principal FindingsIn southern Cameroon, the frequency of two molecular forms–M and S–among which reproductive isolation is strong but still incomplete, was correlated to an index of urbanisation extracted from remotely sensed data, expressed as the proportion of built-up surface in each sampling unit. The two forms markedly segregated along an urbanisation gradient forming a bimodal cline of ∼6-km width: the S form was exclusive to the rural habitat, whereas only the M form was present in the core of densely urbanised settings, co-occurring at times in the same polluted larval habitats of the southern house mosquito Culex quinquefasciatus–a species association that was not historically recorded before.Conclusions/SignificanceOur results indicate that when humans create novel habitats and ecological heterogeneities, they can provide evolutionary opportunities for rapid adaptive niche shifts associated with lineage divergence, whose consequences upon malaria transmission might be significant.

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In contrast to most populations of sexually dimorphic ungulates, a 3-year study revealed a tertiary sex ratio (the number of males per female at sexual maturity) strongly biased towards males in the Île Longue feral sheep (Ovis aries) population (Kerguelen subantarctic archipelago). This population presents a main winter lambing season and a secondary summer lambing period. The sex ratios of lambs and lamb carcasses were even. The skewed sex ratio of adults was therefore attributed to shorter longevity of females. We showed that (i) male monthly mortality followed a bimodal distribution with peaks corresponding to the two rutting periods. Male mortality was, however, highest during the winter even though less rutting occurred in this season than in the summer, suggesting that harsher winter conditions enhance the cost of mating competition; (ii) female mortality was related to the rutting activity of males but not to lambing. Female mortality peaked in the summer despite plentiful food resources. This period corresponds to the main rutting peak, suggesting a high survival cost of mating for females. Female mortality due to male harassment was confirmed by direct observations and examination of females injured during rutting periods. This situation may be due to a strongly male-biased operational sex ratio in the population, associated with an inability of males to establish a stable dominance hierarchy within a large flock.