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  1. 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. 
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  2. 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. 
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  3. 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. 
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  4. 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. 
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  5. A high-resolution map of ant diversity allows an assessment of how well biodiversity centers overlap across taxa. 
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  6. Aim: The standard latitudinal diversity gradient (LDG), in which species richness decreases from equator to pole, is a pervasive pattern observed in most organisms. Some lineages, however, exhibit inverse LDGs. Seemingly problematic, documenting and studying contrarian groups can advance understanding of LDGs generally. Here, we identify one such contrarian clade and use a historical approach to evaluate alternative hypotheses that might explain the group's atypical diversity pattern. We focus on the biogeographical conservatism hypothesis (BCH) and the diversification rate hypothesis (DRH). Location: Global. Taxon: Ants (Hymenoptera: Formicidae: Stenammini). Methods: We examined the shape of the LDG in Stenammini by plotting latitudinal midpoints for all extant, described species. We inferred a robust genome-scale phylogeny using UCE data. We estimated divergence dates using BEAST2 and tested several biogeographical models in BioGeoBEARS. To examine diversification rates and test for a correlation between rate and latitude, we used the programs BAMM and STRAPP, respectively. Results: Stenammini has a skewed inverse LDG with a richness peak in the northern temperate zone. Phylogenomic analyses revealed five major clades and several instances of non-monophyly among genera (Goniomma, Aphaenogaster). Stenammini and all its major lineages arose in the northern temperate zone. The tribe originated ~51 Ma during a climatic optimum and then diversified and dispersed southward as global climate cooled. Stenammini invaded the tropics at least seven times, but these events occurred more recently and were not linked with increased diversification. There is evidence for a diversification rate increase in Holarctic Aphaenogaster + Messor, but we found no significant correlation between latitude and diversification rate generally. Main Conclusions: Our results largely support the BCH as an explanation for the inverse latitudinal gradient in Stenammini. The clade originated in the Holarctic and likely became more diverse there due to center-of-origin, time-for-speciation and niche conservatism effects, rather than latitudinal differences in diversification rate. 
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  7. The monotypic ant genus Igaponera gen. nov. is proposed to include its type species I. curiosa (Mackay & Mackay, 2010). Igaponera gen. nov. is described and phylogenetically compared with other ponerine genera based on external morphology. The type species is known from a single gyne originally described in the genus Pachycondyla Smith, 1858. Igaponera curiosa is easily diagnosed by: costate sculpture on head, mesosoma, and petiole; short, robust, triangular mandibles with blunt apex; relatively large eyes set at mid-length on sides of head; lack of stridulitrum; and presence of distinct but relatively small arolia. Putative apomorphies of the new genus are: cuticular flange concealing metapleural gland opening; vertically standing hypostomal tooth with recessed base; stout mandibular shape with blunt apex; absence of stout spine-like setae on meso- and metatibial apices. Our phylogenetic results based on morphology suggest that Neoponera Emery, 1901 and Pachycondyla are the closest lineages to Igaponera, which shows intermediate characteristics as compared to those genera. The genus is apparently arboreal, known only from a seasonally flooded Igapó forest near Manaus, Brazil. Despite the collection site being frequented by researchers, no other specimens of this genus have been collected in over 40 years prior to this study. 
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  8. Sosa-Calvo, Jeffrey (Ed.)
    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.). 
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  9. Sosa-Calvo, Jeffrey (Ed.)
    Abstract Using genetic, morphological, and geographical evidence, we investigate the species-level taxonomy and evolutionary history of the Pseudomyrmex elongatulus group, a clade of ants distributed from southwestern United States to Costa Rica. Through targeted enrichment of 2,524 UCE (ultraconserved element) loci we generate a phylogenomic data set and clarify the phylogenetic relationships and biogeographic history of these ants. The crown group is estimated to have originated ~8 Ma, in Mexico and/or northern Central America, and subsequently expanded into southern Central America and the southwestern Nearctic. The P. elongatulus group contains a mix of low- and high-elevation species, and there were apparently multiple transitions between these habitat types. We uncover three examples of one species—of restricted or marginal geographical distribution—being embedded phylogenetically in another species, rendering the latter paraphyletic. One of these cases involves an apparent workerless social parasite that occurs sympatrically with its parent species, with the latter serving as host. This suggests a sympatric origin of the parasite species within the distribution range of its host. Species boundaries are tested using three molecular delimitation approaches (SODA, bPTP, BPP) but these methods generate inflated species estimates (26–46 species), evidently because of a failure to distinguish population structure from species differences. In a formal taxonomic revision of the P. elongatulus group, based on almost 3,000 specimens from ~625 localities, we allow for geographic variation within species and we employ distinctness-in-sympatry criteria for testing hypotheses about species limits. Under these guidelines we recognize 13 species, of which nine are new: P. arcanus, sp. nov. (western Mexico); P. capillatus, sp. nov. (western Mexico); P. cognatus, sp. nov. (Chiapas, Mexico to Nicaragua); P. comitator, sp. nov. (Chiapas, Mexico); P. ereptor, sp. nov. (Veracruz, Mexico); P. exoratus, sp. nov. (southeastern Mexico, Honduras); P. fasciatus, sp. nov. (Chiapas, Mexico to Costa Rica); P. nimbus, sp. nov. (Costa Rica); and P. veracruzensis, sp. nov. (Veracruz, Mexico). Our study highlights the value of combining phylogenomic, phenotypic, and geographical data to resolve taxonomic and evolutionary questions. 
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