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Busseola fusca (Lepidoptera: Noctuidae) is an important pest of maize and sorghum in sub-Saharan Africa. One century after its first description by Fuller in 1901, inaccurate information based on earlier reports are still propagated on its distribution (e.g., absent from the lower altitudes in East Africa) and host plant range (e.g., feeding on a large range of wild grass species). This review provides updated information on the biology, distribution and genetics of B. fusca with emphasis on insect-plant interactions. Related to this, new avenues of stem borer management are proposed.

Habitat modification and fragmentation are considered as some of the factors that drive organism distribution and host use diversification. Indigenous African stem borer pests are thought to have diversified their host ranges to include maize [Zea mays L.] and sorghum [Sorghum bicolor (L.) Moench] in response to their increased availability through extensive cultivation. However, management efforts have been geared towards reducing pest populations in the cultivated fields with few attempts to understand possible evolution of "new" pest species. Recovery and growing persistence of Busseola segeta Bowden on maize (Zea mays L.) in Kakamega called for studies on the role of wild host plants on the invasion of crops by wild borer species. A two-year survey was carried out in a small agricultural landscape along the edge of Kakamega forest (Kenya) to assess host range and population genetic structure of B. segeta. The larvae of B. segeta were found on nine different plant species with the majority occurring on maize and sorghum. Of forty cytochrome b haplotypes identified, twenty-three occurred in both wild and cultivated habitats. The moths appear to fly long distances across the habitats with genetic analyses revealing weak differentiation between hosts in different habitats (FST = 0.016; p = 0.015). However, there was strong evidence of variation in genetic composition between growing seasons in the wild habitat (FST = 0.060; p < 0.001) with emergence or disappearance of haplotypes between habitats. Busseola segeta is an example of a phytophagous insect that utilizes plants with a human induced distribution range, maize, but does not show evidence of host race formation or reduction of gene flow among populations using different hosts. However, B. segeta is capable of becoming an important pest in the area and the current low densities may be attributed to the general low infestation levels and presence of a wide range of alternative hosts in the area.

Between the late Oligocene and the early Miocene, climatic changes have shattered the faunal and floral communities and drove the apparition of new ecological niches. Grassland biomes began to supplant forestlands, thus favouring a large-scale ecosystem turnover. The independent adaptive radiations of several mammal lineages through the evolution of key innovations are classic examples of these changes. However, little is known concerning the evolutionary history of other herbivorous groups in relation with this modified environment. It is especially the case in phytophagous insect communities, which have been rarely studied in this context despite their ecological importance. Here, we investigate the phylogenetic and evolutionary patterns of grass-specialist moths from the species-rich tribe Apameini (Lepidoptera, Noctuidae). The molecular dating analyses carried out over the corresponding phylogenetic framework reveal an origin around 29 million years ago for the Apameini. Ancestral state reconstructions indicate (i) a potential Palaearctic origin of the tribe Apameini associated with a major dispersal event in Afrotropics for the subtribe Sesamiina; (ii) a recent colonization from Palaearctic of the New World and Oriental regions by several independent lineages; and (iii) an ancestral association of the tribe Apameini over grasses (Poaceae). Diversification analyses indicate that diversification rates have not remained constant during the evolution of the group, as underlined by a significant shift in diversification rates during the early Miocene. Interestingly, this age estimate is congruent with the development of grasslands at this time. Rather than clade ages, variations in diversification rates among genera better explain the current differences in species diversity. Our results underpin a potential adaptive radiation of these phytophagous moths with the family Poaceae in relation with the major environmental shifts that have occurred in the Miocene.