Leptogenys

Social Hymenoptera show two contrasting strategies of colony reproduction. A reproductive female can raise the first generation of brood alone (independent foundation), or a colony can divide into autonomous parts in which the reproductive female is helped by sterile relatives (fission, budding, swarming). In independent-founding ants, queens can histolize their flight muscles after dispersal; in many species, large flight muscles and metabolic reserves reduce or eliminate the need for risky foraging trips during the vulnerable solitary stage. Colony division is a derived strategy, and we review the selective pressures leading to its occurrence in the different social taxa. In various ants, fission coexists with independent foundation, and alate queens are retained. However, in ants exhibiting obligate fission (e.g. all army ants and many Ponerinae), queens are permanently wingless (ergatoid), or the queen caste is missing altogether. When reproductive females are flightless, dispersal distances and colonization ability are reduced, and there are extensive modifications in mating behavior and resource allocation. We focus on the characteristics of fission in the phylogenetically primitive ants Ponerinae in which both ergatoid queens and gamergates occur. The ground-living habits of ants have permitted extensive changes in the phenotypes of their reproductive females, unlike in wasps and bees.

Recent molecular phylogenetic studies of ants (Hymenoptera: Formicidae) have revolutionized our understanding of how these ecologically dominant organisms diversified, but detailed phylogenies are lacking for most major ant subfamilies. I report the results of the first detailed phylogenetic study of the ant subfamily Ponerinae, a diverse cosmopolitan lineage whose properties make it an attractive model system for investigating social and ecological evolution in ants. Molecular sequence data were obtained from four nuclear genes (wingless, long-wavelength rhodopsin, rudimentary [CAD], 28S rDNA; total of ~3.3 kb) for 86 ponerine taxa, representing all three ponerine tribes, 22 of the 28 currently recognized genera, and 14 of the 18 informal subgenera of Pachycondyla, a heterogeneous grouping whose monophyly is doubtful on morphological grounds. Phylogenetic reconstructions using maximum likelihood and Bayesian inference support the monophyly of Ponerinae and tribe Platythyreini, but fail to support the monophyly of the large tribe Ponerini due to its inclusion of the unusual genus Thaumatomyrmex. Pachycondyla is inferred to be broadly non-monophyletic. Numerous novel generic and suprageneric relationships are inferred within Ponerini, which was found to consist of four major multi-generic clades (the Ponera, Pachycondyla, Plectroctena and Odontomachus genus groups) plus the single genera Hypoponera and Harpegnathos. Uncertainty remains in some regions of the phylogeny, including at the base of Ponerini, possibly reflecting rapid radiation. Divergence dating using a Bayesian relaxed clock method estimates an origin for stem Ponerinae in the upper Cretaceous, a major burst of diversification near the K/T boundary, and a rich and continual history of diversification during the Cenozoic. These results fail to support the predictions of the "dynastic-succession hypothesis" previously developed to explain the high species diversity of Ponerinae. Though model-based reconstructions of historical biogeography and trait evolution were not attempted in this study, the phylogeny suggests that ponerine evolution was marked by regionalized radiations and frequent faunal exchange between major biogeographic provinces. The reported results also imply multiple origins of cryptobiotic foraging, mass raiding behavior, and gamergate reproduction within Ponerinae, highlighting the value of the subfamily as a model for studying the incipient evolution of these and other ecological and behavioral traits.