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Abstract Carpenter ants in the genus Camponotus are large, conspicuous ants that are abundant and ecologically influential in many terrestrial ecosystems. The bicolored carpenter ant, Camponotus vicinus Mayr, is distributed across a wide range of elevations and latitudes in western North America, where it is a prominent scavenger and predator. Here, we present a high-quality genome assembly of C. vicinus from a sample collected in Sonoma County, California, near the type locality of the species. This genome assembly consists of 38 scaffolds spanning 302.74 Mb, with contig N50 of 15.9 Mb, scaffold N50 of 19.9 Mb, and BUSCO completeness of 99.2%. This genome sequence will be a valuable resource for exploring the evolutionary ecology of C. vicinus and carpenter ants generally. It also provides an important tool for clarifying cryptic diversity within the C. vicinus species complex, a genetically diverse set of populations, some of which are quite localized and of conservation interest. 

The arboreal ant genus Tetraponera is widely distributed in the Paleotropics. Five species groups were previously recognized in the Afrotropical region (including Madagascar), and two of these were revised. This paper provides a taxonomic treatment of the remaining species. A survey of the T. allaborans group on the African mainland leads to the recognition of fourteen species: T. clypeata (Emery) (= T. braunsi (Forel) syn. nov.); T. continua (Forel) (= T. claveaui (Santschi) syn. nov.); T. cortina sp. nov.; T. dispar sp. nov.; T. emeryi (Forel) (= T. braunsi durbanensis (Forel) syn. nov.); T. exactor sp. nov.; T. furtiva sp. nov.; T. gerdae (Stitz); T. liengmei (Forel); T. mayri (Forel); T. pedana sp. nov.; T. penzigi (Mayr) (= T. scotti Donisthorpe syn. nov. = T. zavattarii (Menozzi) syn. nov. = T. penzigi praestigiatrix Santschi syn. nov.); T. pumila sp. nov.; and T. tessmanni (Stitz). A full revision of the Malagasy species of the T. allaborans group is deferred, but the following new synonymy is established: T. hysterica (Forel) = T. hysterica inflata (Emery) syn. nov.; T. longula (Emery) = T. sahlbergii deplanata (Forel) syn. nov.; T. mandibularis (Emery) = T. flexuosa (Santschi) syn. nov.; T. morondaviensis (Forel) = T. arrogans (Santschi) syn. nov. = T. demens (Santschi) syn. nov. = T. hysterica dimidiata (Forel) syn. nov.; and T. sahlbergii = T. sahlbergii spuria (Forel) syn. nov. = T. plicatidens (Santschi) syn. nov. In the T. ambigua group the following synonymy is reinstated (syn. rev.): T. ambigua (Emery) = T. erythraea (Emery) = T. bifoveolata (Mayr) = T. angolensis Santschi; and T. ophthalmica (Emery) = T. unidens Santschi. A new species is described in the Madagascar-endemic T. grandidieri group: T. elegans sp. nov. Scrutiny of the T. natalensis group indicates the occurrence of ten species: T. andrei (Mayr), T. anthracina (Santschi), T. caffra (Santschi), T. insularis sp. nov., T. kosi sp. nov., T. mocquerysi (André), T. natalensis (F. Smith), T. redacta sp. nov., T. schulthessi (Santschi), and T. setosa sp. nov. T. insularis is known only from Madagascar, while the other nine species are confined to the African mainland. The following new synonymy is proposed for the T. natalensis group (senior synonym cited first): T. anthracina = T. poultoni Donisthorpe syn. nov. = T. triangularis (Stitz) syn. nov.; T. mocquerysi = T. mocquerysi biozellata (Karavaiev) syn. nov. = T. mocquerysi elongata (Stitz) syn. nov. = T. emacerata (Santschi) syn. nov. = T. triangularis illota (Santschi) syn. nov. = T. ledouxi Terron syn. nov. = T. lemoulti (Santschi) syn. nov. = T. mocquerysi lepida Wheeler syn. nov. = T. monardi (Santschi) syn. nov. = T. emacerata oberbecki (Forel) syn. nov. = T. emacerata odiosa (Forel) syn. nov.; and T. natalensis = T. angusta (Arnold) syn. nov. = T. capensis (F. Smith) syn. nov. = T. natalensis cuitensis (Forel) syn. nov. = T. mocquerysi lutea (Stitz) syn. nov. = T. natalensis obscurata (Emery) syn. nov. = T. prelli (Forel) syn. nov. = T. natalensis usambarensis (Forel) syn. nov. The extensive synonymy under T. mocquerysi and T. natalensis reflects the conviction that previous taxonomists underestimated the extent of intraspecific variation in these taxa, but further study and testing of this conclusion is warranted. An illustrated worker- and queen-based key is provided for all species of Tetraponera occurring in Africa and Madagascar, except the Malagasy members of the T. allaborans group. 

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. 

Camponotus and Colobopsis are widely distributed and species-rich genera in the ant tribe Camponotini. Molecular phylogenetic studies demonstrate that they are not sister taxa, but several lineages within each genus have converged to a remarkable degree, confounding the taxonomy of these ants. Based on multiple lines of evidence, including worker and male morphology, we demonstrate that: (1) three species of “Camponotus” belonging to the subgenus Myrmotemnus, including its type species, are in fact members of the genus Colobopsis ; (2) four species previously assigned to Colobopsis belong to the subgenus Myrmamblys of Camponotus ; and (3) three Nearctic taxa recently placed in Colobopsis are members of the genus Camponotus and closely related to Camponotus clarithorax . These taxonomic findings yield the following new or revived combinations: Colobopsis moeschi ( comb. nov. ), Colobopsis moeschi lygaea ( comb. nov. ), Colobopsis nutans ( comb. nov. ), Colobopsis nutans cleliae ( comb. nov. ), and Colobopsis reichenspergeri ( comb. nov. ); Camponotus apostemata ( comb. nov. ), Camponotus aurelianus ( comb. rev. ), Camponotus cavibregma ( comb. nov. ), Camponotus horrens ( comb. rev. ), Camponotus politae ( comb. rev. ), Camponotus trajanus ( comb. rev. ), and Camponotus yogi ( comb. rev. ). A further consequence is the following generic synonymy (senior synonym listed first): Colobopsis = Myrmotemnus syn. nov. , and Camponotus = Dolophra syn. rev. At the species level, we argue that Camponotus apostemata and Camponotus cavibregma are junior synonyms ( syn. nov. ) of Camponotus yogi , and Camponotus quercicola is a junior synonym ( syn. nov. ) of Ca. laevigatus . Taxonomic comments are also provided on some members of the Camponotus reticulatus group, with Camponotus adustus ( stat. nov. ) and Ca. leucodiscus ( stat. rev. ) being recognized as distinct species rather than subspecies of Ca. bellus . A male-based diagnosis of the Camponotini is provided, and differences between the males of Colobopsis and Camponotus are documented and illustrated for the first time. This study reveals new character systems of potential value to the systematics of these ants, including features of the male genitalia, and emphasizes the value of reciprocal illumination between phylogenomics and critical morphological analysis. 

A high-resolution map of ant diversity allows an assessment of how well biodiversity centers overlap across taxa.