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Abstract The ant genus Tapinoma Foerster, 1850 is a moderately diverse group (81 valid species) that occurs worldwide. It includes the tramp species T. melanocephalum, whose evolutionary history, biogeographic origin, and population limits remain unclear. Here, we present a time-calibrated phylogeny and a biogeographic history inference of the genus based on thousands of Ultraconserved Element (UCE) loci. Focusing on T. melanocephalum, we used single nucleotide polymorphisms from UCE loci and COI sequences to analyze species boundaries based on nuclear and mitochondrial DNA. We recovered a monophyletic Tapinoma with an estimated crown age corresponding to middle Eocene (49.4 to 34.4 Ma). Phylogenomic data differentiated T. melanocephalum from T. jandai, a recently established species based on morphology, and revealed that the 2 species diverged ∼12 Ma. Population genetic analyses identified considerable molecular divergence among sampled T. melanocephalum populations, and a heterogeneous genetic structure, showing a weak relationship between genetic differentiation and geographic distance. A phylogeographic comparison of habitat preferences of T. melanocephalum revealed an ecological shift from undisturbed to urban environments, a phenomenon which may have facilitated its ubiquitous and global distribution. Our study presents the first phylogenomic framework for this globally distributed ant genus and molecularly delineates a worldwide pest ant species. 

Abstract The New World army ants (Hymenoptera: Formicidae) comprise the 5 genera of the Eciton species group, and together they are important keystone predators in tropical and subtropical environments. Generic boundaries in the group have been considered solid and stable for nearly 100 years. Workers of the widespread and diverse genus Neivamyrmex are readily separable from the other 4 genera by lacking a subapical tooth on the tarsal claw, while males can be separated with genitalic characters. The genus Labidus is also widespread and is often abundant, with several species that are conspicuous surface foragers. The least known species of Labidus is L. mars, the workers of which have the tarsal tooth but otherwise share many traits with some Neivamyrmex, being completely eyeless and subterranean. This led us to question its generic placement. Here, we used ultraconserved element (UCE) phylogenomics to show that Labidus mars belongs to the genus Neivamyrmex. All phylogenies, inferred using multiple partitioning schemes and a species tree analysis, recovered the same topology, placing Labidus mars workers within Neivamyrmex. Sequenced males of L. mars were found to be within Labidus and thus incorrectly associated with L. mars. Based on these results and review of key specimens, including types, the following taxonomic changes are made: Neivamyrmex mars (Forel 1912) is a new combination; Labidus nero (Santschi 1930) (rev. stat.) is a male-based taxon revived from synonymy under L. mars; and L. denticulatus (Borgmeier 1955) (new stat.), a male-based taxon and former subspecies of L. mars, is raised to species. 

Temperate zone ants overwinter using a variety of mechanisms. The genusFormicaoverwinters entirely as adults. In at least one species it has been demonstrated that winter workers are more corpulent than summer foragers, storing resources in their bodies and mobilizing them for early brood production in spring. Here we examine overwintering by the common western thatch ant,F. obscuripes. Excavation of a winter nest revealed only workers, distributed in multiple chambers in a roughly spherical region from 0.5 to 1.05 m deep. Worker size, as measured by head width, was weakly bimodal, with fewer workers in the small vs. large size class. We measured dry weights of workers from the winter nest and workers collected the previous summer from the surfaces of multiple nests in the vicinity, including our excavated nest. Controlling for size, there was no evidence of bimodality in winter worker weight, and winter workers were 59.7% heavier than summer foragers. These results suggest thatF. obscuripesworkers are at their maximum corpulence going into their first winter, expend their stored fat during spring, and mostly die before overwintering a second time. It remains uncertain whether workers can regain corpulence. 

Obligatory ant–plant symbioses often appear to be single evolutionary shifts within particular ant lineages; however, convergence can be revealed once natural history observations are complemented with molecular phylogenetics. Here, we describe a remarkable example of convergent evolution in an ant–plant symbiotic system. Exclusively arboreal,Myrmelachistaspecies can be generalized opportunists nesting in several plant species or obligately symbiotic, live-stem nesters of a narrow set of plant species. Instances of specialization withinMyrmelachistaare known from northern South America and throughout Middle America. In Middle America, a diverse radiation of specialists occupies understory treelets of lowland rainforests. The morphological and behavioural uniformity of specialists suggests that they form a monophyletic assemblage, diversifying after a single origin of specialization. Using ultraconserved element phylogenomics and ancestral state reconstructions, we show that shifts from opportunistic to obligately symbiotic evolved independently in South and Middle America. Furthermore, our analyses support a remarkable case of convergence within the Middle American radiation, with two independently evolved specialist clades, arising nearly simultaneously from putative opportunistic ancestors during the late Pliocene. This repeated evolution of a complex phenotype suggests similar mechanisms behind trait shifts from opportunists to specialists, generating further questions about the selective forces driving specialization. 

The genus-level classification of the ant subfamily Ponerinae (Hymenoptera: Formicidae) is revised based on a comprehensive phylogenomic analysis of more than 2,300 ultraconserved element (UCE) loci across 1,170 sampled specimens representing 1,020 taxa (600 valid species and 420 morphospecies) and all described ponerine genera known from workers. While most previously defined genus groups are recovered as monophyletic, several genera are shown to be polyphyletic or paraphyletic. To resolve these inconsistencies, four new genera are described:Boltonoponegen. nov.,Makebaponegen. nov.,Subiridoponegen. nov., andSritoponeragen. nov.Xiphopeltastat. rev.is revalidated andEuponerais restricted by expandingFisheroponeto absorb a paraphyletic assemblage.Mesoponerais split into four lineages, resulting in transfers toMakebapone,Subiridopone, andXiphopelta.Iroponerasyn. nov.is synonymized underCryptoponeand additional new synonymies at both the generic and species levels are established. Morphological diagnoses are revised for each affected genus, and updated species lists and new combinations are provided. The updated classification recognizes 54 valid genera within Ponerinae and acknowledges an additional lineage that will be formally described in a subsequent publication. To support identification and comparative studies, revised keys to all extant Ponerinae genera are provided, presented by biogeographic region (African and Malagasy, Palearctic–Indomalaya–Australasia, and New World). This classification is intended to provide a stable, phylogenetically informed framework for future research on ponerine ants. 

Abstract The genus Cryptopone Emery contains 25 species of litter and soil ants, 5 of which occur in the Americas. Cryptopone gilva (Roger) occurs in the southeastern United States and cloud forests of Mesoamerica, exhibiting an uncommon biogeographic disjunction observed most often in plants. We used phylogenomic data from ultraconserved elements (UCEs), as well as mitogenomes and legacy markers, to investigate phylogenetic relationships, species boundaries, and divergence dates among New World Cryptopone. Species delimitation was conducted using a standard approach and then tested using model-based molecular methods (SNAPP, BPP, SODA, and bPTP). We found that Cryptopone as currently constituted is polyphyletic, and that all the South American species belong to Wadeura Weber, a separate genus unrelated to Cryptopone. A single clade of true Cryptopone occurs in the Americas, restricted to North and Central America. This clade is composed of four species that originated ~4.2 million years ago. One species from the mountains of Guatemala is sister to the other three, favoring a vicariance hypothesis of diversification. The taxonomy of the New World Cryptopone and Wadeura is revised. Taxonomic changes are as follows: Wadeura Weber is resurrected, with new combinations W. guianensis Weber, W. holmgreni (Wheeler), and W. pauli (Fernandes & Delabie); C. guatemalensis (Forel) (rev. stat.) is raised to species and includes C. obsoleta (Menozzi) (syn. nov.). The following new species are described: Cryptopone gilvagrande, C. gilvatumida, and Wadeura holmgrenita. Cryptopone hartwigi Arnold is transferred to Fisheropone Schmidt and Shattuck (n. comb.). Cryptopone mirabilis (Mackay & Mackay 2010) is a junior synonym of Centromyrmex brachycola (Roger) (syn. nov.). 

Abstract The ant genus Syscia  Roger, 1861 is part of the cryptic ant fauna inhabiting leaf litter and rotten wood in the Asian and American tropics. It is a distinct clade within the Dorylinae, the subfamily from which army ants arose. Prior to this work, the genus comprised seven species, each known from a single or very few collections. Extensive collecting in Middle America revealed an unexpected and challenging diversity of morphological forms. Locally distinct forms could be identified at many sites, but assignment of specimens to species spanning multiple sites was problematic. To improve species delimitation, Ultra-Conserved Element (UCE) phylogenomic data were sequenced for all forms, both within and among sites, and a phylogeny was inferred. Informed by phylogeny, species delimitation was based on monophyly, absence of within-clade sympatry, and a subjective degree of morphological uniformity. UCE phylogenomic results for 130 specimens were complemented by analysis of mitochondrial COI (DNA barcode) data for an expanded taxon set. The resulting taxonomy augments the number of known species in the New World from 3 to 57. We describe and name 31 new species, and 23 species are assigned morphospecies codes pending improved specimen coverage. Queens may be fully alate or brachypterous, and there is a wide variety of intercaste female forms. Identification based on morphology alone is very difficult due to continuous character variation and high similarity of phylogenetically distant species. An identification aid is provided in the form of a set of distribution maps and standard views, with species ordered by size. 

Taxonomy is the business of describing and naming organismal diversity. What that means exactly must shift as our conceptual framework shifts (as it did during the time of Darwin) and as what we are able to see shifts as a result of technological assists. We are at a moment of profound conceptual and technological change. Here I give some personal thoughts on three top questions in taxonomy. Are traditional naming conventions compatible with massive cryptic genetic discontinuity? Can we agree on what we are delimiting and naming?  Can we excite public interest without typology?