The evolution of multiple mating in army ants

The evolution of mating systems in eusocial Hymenoptera is constrained because females mate only during a brief period early in life, whereas inseminated queens and their stored sperm may live for decades. Considerable research effort during recent years has firmly established that obligate multiple mating has evolved only a few times: in Apis honeybees, Vespula wasps, Pogonomyrmex harvester ants, Atta and Acromyrmex leaf-cutting ants, the ant Cataglyphis cursor, and in at least some army ants. Here we provide estimates of queen-mating frequency for New World Neivamyrmex and Old World Aenictus species, which, compared to other army ants, have relatively small colonies and little size polymorphism among workers. To provide the first overall comparative analysis of the evolution of army ant mating systems, we combine these new results with previous estimates for African Dorylus and New World Eciton army ants, which have very large colonies and considerable worker polymorphism. We show that queens of Neivamyrmex and Aenictus mate with the same high numbers of males (usually ca. 10-20) as do queens of army ant species with very large colony sizes. We infer that multiple queen mating is ancestral in army ants and has evolved over 100 million years ago as part of the army ant adaptive syndrome. A comparison of army ants and honeybees suggests that mating systems in these two distantly related groups may have been convergently shaped by strikingly similar selective pressures.     

Fine structure of the postpygidial gland in Aenictus army ants

Billen, J., Gobin, B. & Ito, F. 1999. Fine structure of the postpygidial gland in Aenictus army ants. – Acta Zoologica (Stockholm) 80: 307–310
Army ants of the genus Aenictus are characterized by the presence of a conspicuous postpygidial gland, which is the source of the trail pheromone. The paired gland at each side consists of a reservoir sac into which the secretory cells open through their accompanying duct cells. The secretory cells are characterized by a well developed Golgi apparatus, numerous mitochondria and strands of smooth endoplasmic reticulum. The reservoir opens near the abdomen tip, which facilitates deposition of the secretory products onto the substrate. The large reservoir of the postpygidial gland may enable the incessant trail laying of at least one of the investigated species.     

Extraordinary Predation by the Neotropical Army Ant Cheliomyrmex andicola: Implications for the Evolution of the Army Ant Syndrome1

Workers of the genus Cheliomyrmex are unique among the New world army ants (subfamily Ecitoninae) in that their mandibles are armed with elongate, spine‐like teeth. We present the first prey records for this genus. Cheliomyrmex andicola prey on large‐bodied ground dwelling invertebrates and, possibly, on vertebrates. Unlike other army ants, C. andicola workers use their sting during prey capture. The workers' unusual mandibles and potent stings may be adapted for piercing and gripping the integument of nonarthropod prey animals, and for rapidly subduing large‐bodied prey, respectively. The genus Cheliomyrmex may be the sister taxon to other Neotropical army ants (Ecitoninae), and Cheliomyrmex shares features of mandibular morphology and prey selection with Old World driver ants in the genus Dorylus. Mass cooperative foraging, an important element of army ant behavior, may have arisen in part as an adaptation for exploiting large‐bodied prey.     

Species‐level predation network uncovers high prey specificity in a Neotropical army ant community

Army ants are among the top arthropod predators and considered keystone species in tropical ecosystems. During daily mass raids with many thousand workers, army ants hunt live prey, likely exerting strong top‐down control on prey species. Many tropical sites exhibit a high army ant species diversity (>20 species), suggesting that sympatric species partition the available prey niches. However, whether and to what extent this is achieved has not been intensively studied yet. We therefore conducted a large‐scale diet survey of a community of surface‐raiding army ants at La Selva Biological Station in Costa Rica. We systematically collected 3,262 prey items from eleven army ant species (genera Eciton, Nomamyrmex and Neivamyrmex). Prey items were classified as ant prey or non‐ant prey. The prey nearly exclusively consisted of other ants (98%), and most booty was ant brood (87%). Using morphological characters and DNA barcoding, we identified a total of 1,103 ant prey specimens to the species level. One hundred twenty‐nine ant species were detected among the army ant prey, representing about 30% of the known local ant diversity. Using weighted bipartite network analyses, we show that prey specialization in army ants is unexpectedly high and prey niche overlap very small. Besides food niche differentiation, we uncovered a spatiotemporal niche differentiation in army ant raid activity. We discuss competition‐driven multidimensional niche differentiation and predator–prey arms races as possible mechanisms underlying prey specialization in army ants. By combining systematic prey sampling with species‐level prey identification and network analyses, our integrative approach can guide future research by portraying how predator–prey interactions in complex communities can be reliably studied, even in cases where morphological prey identification is infeasible.     

How much do army ants eat? On the prey intake of a neotropical top-predator

New World army ants (Ecitoninae) are nomadic group-predators that are widely thought to have a substantial impact on their prey. Nevertheless, quantitative data on prey intake by army ants is scarce and mostly limited to chance encounters. Here, I quantify the prey intake of the army ant Eciton hamatum at the contrasting scales of raid, colony (sum of simultaneous raids), and population. Like most army ants, E. hamatum conducts narrow ‘column raids’ and has a specialized diet of ant prey. I show that individual raids often had periods of no prey intake, and raid intake rates, calculated in g/min, differed significantly among colonies. Moreover, neither mean nor peak raid intake rates were correlated with colony size. Similarly, colony intake rates differed significantly among colonies, and mean colony intake rates were not correlated with colony size. However, mean colony intake rates were significantly higher than mean raid intake rates, and peak colony intake rate was correlated with colony size. Having multiple raids thus improves colony-level intake rates, and larger colonies can harvest more prey per unit time. Mean colony intake rate across colonies was 0.067 g/min dry weight and mean daily colony intake was calculated at 38.2 g. This intake is comparable to that of Eciton burchellii, which has a more generalized diet and conducts spectacular ‘swarm raids’ that are seen as having a greater impact on prey than column raids. Population size on Barro Colorado Island, Panama, was estimated to be 57 colonies, which extrapolates to a daily population intake of nearly 2 kg of prey dry weight, or 120 g/km². Broadly, these findings demonstrate that column raiding army ants experience considerable variation in prey intake for individual raids, but can still achieve notable impact at the larger scales of colony and population. Furthermore, they challenge the idea that swarm-raiding species necessarily have greater intake and thus impact on prey. Instead, I suggest that conducting multiple column raids may be a strategy that allows for comparable intake from a more specialized diet.     

Isolation and characterization of eight microsatellite loci in two morphotypes of the Southeast Asian army ant,Aenictus laeviceps

Eight polymorphic microsatellite markers were developed from morphotype L1 of the Southeast Asian army ant, Aenictus laeviceps in Borneo, and characterized for morphotypes L1 and L2. The number of alleles per locus ranged from nine to 24 (average 15) in morphotype L1 and two to 16 (average 9.8) in L2. Observed heterozygosity ranged from 0.75 to 0.96 in morphotype L1 and from 0.08 to 0.96 in L2. All loci were in Hardy–Weinberg equilibrium. One pair of loci showed linkage disequilibrium in morphotype L1. All markers successfully amplified in morphotype S, and some markers amplified in other Aenictus species.     

Morphological phylogeny of army ants and other dorylomorphs (Hymenoptera: Formicidae)

Abstract. The dorylomorph group of ants comprises the three subfamilies of army ants (Aenictinae, Dorylinae, Ecitoninae) together with the subfamilies Aenictogitoninae, Cerapachyinae, and Leptanilloidinae. We describe new morphological characters and synthesize data from the literature in order to present the first hypothesis of phylogenetic relationships among all dorylomorph genera. These data include the first available character information from the newly discovered male caste of Leptanilloidinae. We used ant taxa from Leptanillinae, Myrmeciinae, and the poneromorph (Ponerinae sensu lato) subfamilies Amblyoponinae, Ectatomminae, and Paraponerinae as outgroups. We scored a total of 126 characters from twenty-two terminal taxa and used these data to conduct maximum parsimony and bootstrap analyses. The single most-parsimonious tree and bootstrap results support a single origin of army ants. The Old World army ant genus Dorylus forms a monophyletic group with the enigmatic genus Aenictogiton, which is currently known only from males; the second Old World army ant genus Aenictus is sister to this clade. This result generates the prediction that females of Aenictogiton, when discovered, will be observed to possess the army ant syndrome of behavioural and reproductive traits. The monophyly of the New World army ants (Ecitoninae) is supported very strongly, and within this group the genera Eciton, Nomamyrmex, and Labidus form a robust clade. The monophyly of Leptanilloidinae is also upheld. The subfamily Cerapachyinae appears paraphyletic, although this conclusion is not supported by strong bootstrap results. Relationships among genera of Cerapachyinae similarly are not resolved robustly, although parsimony results suggest clades consisting of (Acanthostichus + Cylindromyrmex) and (Cerapachys + Sphinctomyrmex). We tested for the effect of incompletely known taxa by conducting a secondary analysis in which the two genera containing ∼50% missing character data (Aenictogiton and Asphinctanilloides) were removed. The strict consensus of the seventeen most-parsimonious trees from this secondary analysis is poorly resolved outside the army ants and contains no clades conflicting with the primary analysis. The position of Leptanilla shifts from forming the sister group to Leptanilloidinae (without high bootstrap support) in the primary analysis, to falling within a polytomy at the base of the root of the dorylomorphs when incompletely known taxa are removed. This instability suggests that the placement of Leptanilla within the dorylomorphs in our primary analysis may be spurious.     

Do army ant queens re-mate later in life?

Queens of eusocial Hymenoptera are inseminated only during a brief period before they start to lay eggs. This has probably been kin-selected because repeated insemination of old queens would normally be against the inclusive fitness interest of their daughter workers. Army ants have been considered to be the only possible exception to this rule due to their idiosyncratic life-history. We studied two distantly related species of army ants, the African Dorylus (Anomma) molestus and the Neotropical Eciton burchellii and present data from microsatellite genotyping, behavioural observations and sperm counts.We also describe the copulation behaviour of African army ants for the first time. Our results strongly suggest that, contradictory to earlier contentions, army ant queens do not mate repeatedly throughout their life and thus do not constitute an exception among the eusocial Hymenoptera in this respect. Sperm counts for males and queens of both species show that army ant queens have to mate with several males to become fully inseminated. However, sperm limitation by queens is unlikely to have been the prime reason for the evolution of high queen-mating frequencies in this group. Received 5 July 2006; revised 26 September 2006; accepted 11 October 2006.     

Birds and army ants in a fragment of the Atlantic Forest of Brazil

ABSTRACT Little is known about the birds associated with army‐ant swarms in the Brazilian Atlantic forest. Our objectives were to locate and monitor army‐ant swarms in the Atlantic rainforest of Brazil and to identify the species of birds that attended the swarms and exhibited bivouac‐checking behavior. From July 2004 to August 2005, we located 49 swarms of army ants, including 28 Eciton burchelli, 19 Labidus praedator, and 2 Eciton vagans swarms. No birds were present at 17 (35%) swarms. At 32 swarms where birds were present, 22 (69%) were E. burchelli swarms and 10 (31%) were L. praedator swarms. No birds were observed at the two E. vagans swarms. We identified 66 species of birds attending the swarms, but only 43 species were observed foraging on prey flushed by the ants. Eighteen of these species had not been previously reported to forage in association with army‐ant swarms. Most birds observed during our study attended army‐ant swarms opportunistically, with White‐shouldered Fire‐eyes (Pyriglena leucoptera) the only obligate ant follower. Our observations suggest that the arthropods and other organisms flushed by army ants represent an important food resource for several species of birds in the Atlantic forest ecosystem.     

A molecular phylogeny of <Emphasis Type="Italic">Dorylus</Emphasis> army ants provides evidence for multiple evolutionary transitions in foraging niche

Background  

Army ants are the prime arthropod predators in tropical forests, with huge colonies and an evolutionary derived nomadic life style. Five of the six recognized subgenera of Old World Dorylus army ants forage in the soil, whereas some species of the sixth subgenus (Anomma) forage in the leaf-litter and some as conspicuous swarm raiders on the forest floor and in the lower vegetation (the infamous driver ants). Here we use a combination of nuclear and mitochondrial DNA sequences to reconstruct the phylogeny of the Dorylus s.l. army ants and to infer the evolutionary transitions in foraging niche and associated morphological adaptations.     

Elevational and geographic variation in army ant swarm raid rates

Geographic and elevational variation in the local abundance of swarm-raiding army ants has implications for the population dynamics of their prey, as well as affecting the profitability of army-ant-following behavior for birds. Here, we analyze systematically collected data on E. burchellii and L. praedator raid rates from geographically and elevationally wide-ranging sites, from lowland to montane forests. We show that raids of each species, and of both species pooled, reach peak densities at intermediate (premontane) elevations. These patterns suggest that army ant swarm raids are relatively abundant in Neotropical montane forests. Therefore, a paucity of ant raids does not explain the absence of obligate ant-following bird species, particularly true antbirds (Thamnophilidae), from montane forests. As army ant raids are relatively common at middle elevations, opportunities exist for other montane bird taxa to exploit army ant raids as a food source.     

Complex Nesting Behavior by Two Neotropical Species of the Ant Genus Stenamma (Hymenoptera: Formicidae)1

Two Neotropical ant species, Stenamma expolitum Smith and S. alas new species (described here), exhibit three unusual nesting behaviors: (1) they build architecturally sophisticated nest entrances that elevate the nest opening away from the surface; (2) they maintain multiple identical nests but occupy only one of them; and (3) they keep a round “door pebble” at the nest entrance, with which they plug the opening in response to army ants. Adaptive hypotheses for these behaviors are discussed, including the possibility that there are multiple lines of defense against army ant predation.     

A new species of the Aenictus wroughtonii group (Hymenoptera,Formicidae) from South-East China

A new species of army ant from the Aenictus wroughtonii group is described and illustrated based on the worker caste. Aenictus gutianshanensis Staab, sp. n. is known form a single colony collected in the subtropical mixed evergreen broad-leaved forest of the Gutianshan National Nature Reserve, South-East China. The new species is probably most closely related to A. vieti Jaitrong & Yamane, 2010 known from North Vietnam and Taiwan. It is suggested that the abundant records of A. camposi Wheeler & Chapman, 1925 from East and South-East China should be reevaluated, as they are probably A. gutianshanensis or A. vieti and not A. camposi, which is distributed in Sundaland, the Philippines, and the southernmost part of continental South-East Asia.     

Army ant invasions reveal phylogeographic processes across the Isthmus of Panama

Female army ants cannot fly, making them very poor dispersers across water barriers. This dependence on terrestrial corridors motivated the investigation by Winston et al. ( 2017 ), published in this issue of Molecular Ecology, into the role of Panamanian isthmus formation in the diversification of Eciton army ants. Complete closure of this isthmus occurred around three million years ago (3 Ma), but it has also been hypothesized that earlier, temporary land connections facilitated additional colonization events between South and Central America over the past 13 million years or more. The phylogenomic and population genomic analyses by Winston et al. ( 2017 ) uncovered multiple incursions of Eciton lineages into Central America between 4 and 7 Ma. Their study contributes to a growing body of evidence arguing that transitory land bridges predating 3 Ma supported substantial intercontinental biotic exchange.     

Observations of Strange-tailed Tyrants (Alectrurus risora) and other grassland birds following army ants and armadillos

ABSTRACT.   Birds in Neotropical forests frequently follow army ants to forage for insects. Here we report the first record of several species of Neotropical grassland birds following army ants ( Labidus praedator ) and yellow armadillos ( Euphractus sexcinctus ). We observed Strange-tailed Tyrants ( Alectrurus risora ) following army ants in El Bagual Ecological Reserve in Argentina. Other species also observed following army ants included Pampas Finches ( Embernagra platensis ), Wedge-tailed Grass-finches ( Emberizoides herbicola ), Long-tailed Reed-finches ( Donacospiza albifrons ), Great Kiskadees ( Pitangus sulphuratus ), Rufous Horneros ( Furnarius rufus ), Gray Monjitas ( Xolmis cinerea ), and Pale-breasted Spinetails ( Synallaxis albescens ). Strange-tailed Tyrants and Wedge-tailed Grass-finches were also observed following armadillos. Because birds were observed capturing insects flushed by the army ants and armadillos, our observations indicate that birds that opportunistically follow army ants and armadillos benefit from the association.     

The structured diversity of specialized gut symbionts of the New World army ants

Symbiotic bacteria play important roles in the biology of their arthropod hosts. Yet the microbiota of many diverse and influential groups remain understudied, resulting in a paucity of information on the fidelities and histories of these associations. Motivated by prior findings from a smaller scale, 16S rRNA‐based study, we conducted a broad phylogenetic and geographic survey of microbial communities in the ecologically dominant New World army ants (Formicidae: Dorylinae). Amplicon sequencing of the 16S rRNA gene across 28 species spanning the five New World genera showed that the microbial communities of army ants consist of very few common and abundant bacterial species. The two most abundant microbes, referred to as Unclassified Firmicutes and Unclassified Entomoplasmatales, appear to be specialized army ant associates that dominate microbial communities in the gut lumen of three host genera, Eciton, Labidus and Nomamyrmex. Both are present in other army ant genera, including those from the Old World, suggesting that army ant symbioses date back to the Cretaceous. Extensive sequencing of bacterial protein‐coding genes revealed multiple strains of these symbionts coexisting within colonies, but seldom within the same individual ant. Bacterial strains formed multiple host species‐specific lineages on phylogenies, which often grouped strains from distant geographic locations. These patterns deviate from those seen in other social insects and raise intriguing questions about the influence of army ant colony swarm‐founding and within‐colony genetic diversity on strain coexistence, and the effects of hosting a diverse suite of symbiont strains on colony ecology.     

First record of the ant subfamily Aenictinae (Hymenoptera,Formicidae) from Saudi Arabia,with?the description of a new species

The ant subfamily Aenictinae is recorded for the first time from the Kingdom of Saudi Arabia and for the second time from the Arabian Peninsula. A new species Aenictus arabicus sp. n., is described from the worker caste. Aenictus arabicus belongs to the Aenictus wroughtonii-group and appears to be most closely related to Aenictus rhodiensis Menozzi, but can be easily distinguished from the latter by the following characters: overall smaller size; cephalic index (head width/head length) small; occipital corners in lateral view rounded; antennal scape when laid back surpassing approximately two-thirds of head length; funicular segments 2–8 each at least 2× as long as broad; subpetiolar process well developed; petiole and postpetiole distinctly imbricate; gaster and clypeus entirely yellow, teeth of mandibles reddish- brown. Aenictus arabicus was collected from leaf litter, next to a tree of Psidium guajava L. The new species also is similar to Aenictus sagei and Aenictus wroughtonii. Affinities and a key to related species of the species group are given.     

Combat between large derived societies: A subterranean army ant established as a predator of mature leaf-cutting ant colonies

Summary. Mature colonies of Atta leaf-cutting ants are dominant herbivores throughout the Neotropics. Although young colonies have natural enemies, mature colonies, which live in extensive nests containing millions of workers, currently have no recognised predators. New World army ants (Ecitoninae) are specialist social predators of other ants, and the army ant Nomamyrmex esenbeckii, a primarily subterranean species, is known to prey upon young Atta colonies. Here we present the results of the first long-term study of the predator-prey interaction between N. esenbeckii and Atta. Our study establishes the army ant N. esenbeckii as the only known predator capable of successfully attacking and killing mature as well as young colonies of Atta leaf-cutting ants. In natural raids, and experimental tests, Atta rapidly recruited their largest workers (majors) as a specific defensive response to N. esenbeckii raiders and both taxa used their largest individuals in the frontline of battles. The deployment and behaviour of these large workers demonstrates a size-related division of labour and agrees with the predictions of Lanchesters Linear Law of Combat. Both taxa also used cooperative combat teams to overwhelm large combatants from the other side. The success of N. esenbeckii raids varied greatly, such that they were prevented from entering Atta nests in the least successful raids, and completely overran Atta colonies in the most successful raids. The speed and magnitude of the defensive response of mature Atta colonies was key in determining the level of success of N. esenbeckii raids.Received 12 December 2003; revised 25 March 2004; accepted 1 April 2004.Work conducted at the Smithsonian Tropical Research Institute, Apartado 2072, Balboa, Ancon, Republic of Panama     

Chimpanzees prey on army ants with specialized tool set

Several populations of chimpanzees have been reported to prey upon Dorylus army ants. The most common tool‐using technique to gather these ants is with “dipping” probes, which vary in length with regard to aggressiveness and lifestyle of the prey species. We report the use of a tool set in army ant predation by chimpanzees in the Goualougo Triangle, Republic of Congo. We recovered 1,060 tools used in this context and collected 25 video recordings of chimpanzee tool‐using behavior at ant nests. Two different types of tools were distinguished based on their form and function. The chimpanzees use a woody sapling to perforate the ant nest, and then a herb stem as a dipping tool to harvest the ants. All of the species of ants preyed upon in Goualougo are present and consumed by chimpanzees at other sites, but there are no other reports of such a regular or widespread use of more than one type of tool to prey upon Dorylus ants. Furthermore, this tool set differs from other types of tool combinations used by chimpanzees at this site for preying upon termites or gathering honey. Therefore, we conclude that these chimpanzees have developed a specialized method for preying upon army ants, which involves the use of an additional tool for opening nests. Further research is needed to determine which specific ecological and social factors may have shaped the emergence and maintenance of this technology. Am. J. Primatol. 72:17–24, 2010. © 2009 Wiley‐Liss, Inc.