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A new collection of 24 wingless ant specimens from mid-Cretaceous Burmese amber (Albian-Cenomanian, 99 Ma) comprises nine new species belonging to the genus Sphecomyrmodes Engel and Grimaldi. Described taxa vary considerably with regard to total size, head and body proportion, cuticular sculpturing, and petiole structure while all species are unified by a distinct shared character. The assemblage represents the largest known diversification of closely related Cretaceous ants with respect to species number. These stem-group ants exhibit some characteristics previously known only from their extant counterparts along with presumed plesiomorphic morphology. Consequently, their morphology may inform hypotheses relating to basal relationships and general patterns of ant evolution. These and other uncovered Cretaceous species indicate that stem-group ants are not simply wasp-like, transitional formicids, but rather a group of considerable adaptive diversity, exhibiting innovations analogous to what crown-group ants would echo 100 million years later.

The concerted evolution of morphological and behavioral specializations has compelling examples in ant castes. Unique to ants is a marked divergence between winged queens and wingless workers, but morphological specializations for behaviors on the ground have been overlooked. We analyzed thorax morphology of queens and workers in species from 21 of the 25 ant subfamilies. We uncovered unique skeletomuscular modifications in workers that presumably increase power and flexibility of head–thorax articulation, emphasizing that workers are not simply wingless versions of queens. We also identified two distinct types of queens and showed repeated evolutionary associations with strategies of colony foundation. Solitary founding queens that hunt have a more worker-like thorax. Our results reveal that ants invest in the relative size of thorax segments according to their tasks. Versatility of head movements allows for better manipulation of food and objects, which arguably contributed to the ants’ ecological and evolutionary success. The size and shape of an animal, known as its morphology, often reflect the actions it can perform. A grasshopper’s long legs, for example, are well suited to hopping, whilst the streamlined body of a dolphin helps swimming through water. These specialized features result from the interplay between morphology and behavior during evolution. A change in morphology can make new behaviors possible, which can then expose the animal to new environments and selective pressures that, in turn, can lead to further changes in morphology. The interplay between morphology and behavior is particularly interesting in social insects such as ants. Queens and workers within an ant colony have a similar set of genes, but they have dramatically different morphologies and very different roles within the colony. Queens are responsible for reproduction, and are larger and have wings, which allow them to fly and establish a new colony away from where they were born. Workers are smaller and lack wings, and they devote themselves to building the nest, feeding the young larvae and protecting the colony. This marked morphological divergence, unique to ants, has fascinated researchers for more than a century. However, most studies have focused on the presence or absence of wings and have overlooked the interactions between morphology and the actions performed on the ground. Like all insects, an ant’s body is divided into three parts: the head, the thorax (to which the legs and wings are attached), and the abdomen. Now, Keller et al. have examined the shape of the thorax in many species of ants and found that workers are not just smaller wingless versions of queens: rather, the architecture of their thorax is unique among species of flying insects. The front end of the worker thorax is greatly enlarged and is filled by strong neck muscles that power the head and its jaws, and allow workers to hunt and carry prey many times their own weight. Keller et al. also identified two distinct types of queens and went on to show that these two shapes evolved in association with the two types of strategy that lone queens use to found new colonies. In species where queens convert their own wing muscles into the food for the first generation of workers, the wing muscles are much enlarged and the neck segment is extremely reduced. In species where queens hunt to feed the new colony, the wing and neck muscles are more balanced in size. As such, for those ant species where very little is known about how new colonies are founded, Keller et al. show that we can use the shape of the queen’s thorax to help predict this behavior. Taken together, the results of Keller et al. show that female ants invest in the relative size of the different segments of the thorax in a way that reflects their behavior as adults. These adaptations partly explain why ants have been so extraordinarily successful in nature, and underscore the importance of carefully analyzing an organism’s form to fully understand its biology.

Recent studies on the ant phylogeny are mainly based on the molecular analyses of extant subfamilies and do not include the extinct, only Cretaceous subfamily Sphecomyrminae. However, the latter is of major importance for ant relationships, as it is considered the most basal subfamily. Therefore, each new discovery of a Mesozoic ant is of high interest for improving our understanding of their early history and basal relationships. In this paper, a new sphecomyrmine ant, allied to the Burmese amber genus Haidomyrmex, is described from mid-Cretaceous amber of France as Haidomyrmodes mammuthus gen. and sp. n. The diagnosis of the tribe Haidomyrmecini is emended based on the new type material, which includes a gyne (alate female) and two incomplete workers. The genus Sphecomyrmodes, hitherto known by a single species from Burmese amber, is also reported and a new species described as S. occidentalis sp. n. after two workers remarkably preserved in a single piece of Early Cenomanian French amber. The new fossils provide additional information on early ant diversity and relationships and demonstrate that the monophyly of the Sphecomyrminae, as currently defined, is still weakly supported.