Enforced specificity of an animal symbiosis.

Insect diversification has been catalyzed by widespread specialization on novel hosts - a process underlying exceptional radiations of phytophagous beetles, lepidopterans, parasitoid wasps, and inordinate lineages of symbionts, predators and other trophic specialists. The strict fidelity of many such interspecies associations is posited to hinge on sensory tuning to host-derived cues, a model supported by studies of neural function in host-specific model species. Here, we investigated the sensory basis of symbiotic interactions between a myrmecophile rove beetle and its single, natural host ant species.

The genomic and cellular basis of biosynthetic innovation in rove beetles.

How evolution at the cellular level potentiates macroevolutionary change is central to understanding biological diversification. The >66,000 rove beetle species (Staphylinidae) form the largest metazoan family. Combining genomic and cell type transcriptomic insights spanning the largest clade, Aleocharinae, we retrace evolution of two cell types comprising a defensive gland-a putative catalyst behind staphylinid megadiversity.

The genomic and cellular basis of biosynthetic innovation in rove beetles.

How evolution at the cellular level potentiates change at the macroevolutionary level is a major question in evolutionary biology. With >66,000 described species, rove beetles (Staphylinidae) comprise the largest metazoan family. Their exceptional radiation has been coupled to pervasive biosynthetic innovation whereby numerous lineages bear defensive glands with diverse chemistries.

Parallel evolutionary paths of rove beetle myrmecophiles: replaying a deep-time tape of life.

The rise of ants over the past ~100 million years reshaped the biosphere, presenting ecological challenges for many organisms, but also opportunities. No insect group has been so adept at exploiting niches inside ant colonies as the rove beetles (Staphylinidae) - a global clade of>64,000 predominantly free-living predators from which numerous socially parasitic 'myrmecophile' lineages have emerged. Myrmecophilous staphylinids are specialized for colony life through changes in behavior, chemistry, anatomy, and life history that are often strikingly convergent, and hence potentially adaptive for this symbiotic way of life.