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Elevational gradients provide an interesting opportunity for studying the effect of climatic drivers over short distances on the various facets of biodiversity. It is globally assumed that the decrease in species richness with increasing elevation follows mainly the decrease in ecosystem productivity, but studies on functional diversity still remain limited. Here, we investigated how resource use and food preferences by both individual ant species and communities foraging in the understory vary with elevation along a complete elevational gradient (200 to 3200 m asl). Five bait types reflecting some of the main ecosystem processes in which ants are involved were tested: mutualism (sucrose and melezitose), predation (live termites), and detritivory (crushed insects and chicken feces). The observed monotonic decrease in both species richness and occurrences with elevation increase was accompanied by changes in some of the tested ecosystem processes. Such variations can be explained by resource availability and/or resource limitation: Predation and bird feces removal decreased with increasing elevation possibly reflecting a decline in species able to use these resources, while insect detritivory and nectarivory were most probably driven by resource limitation (or absence of limitation), as their relative use did not change along the gradient. Consequently, resource attractiveness (i.e., food preferences at the species level) appears as an important factor in driving community structuring in ants together with the abiotic environmental conditions.

The plant Hirtella physophora, the ant Allomerus decemarticulatus and a fungus, Trimmatostroma sp., form a tripartite association. The ants manipulate both the plant trichomes and the fungus to build galleries under the stems of their host plant used to capture prey. In addition to its structural role, the fungus also improves nutrient uptake by the host plant. But it still remains unclear whether the fungus plays an indirect or a direct role in transferring nutrients to the plant. This study aimed to trace the transfer of N from the fungus to the plant's stem tissue. Optical microscopy and transmission electron microscopy (TEM) were used to investigate the presence of fungal hyphae in the stem tissues. Then, a 15N-labelling experiment was combined with a nanoscale secondary-ion mass spectrometry (NanoSIMS 50) isotopic imaging approach to trace the movement of added 15N from the fungus to plant tissues. The TEM images clearly showed hyphae inside the stem tissue in the cellular compartment. Also, fungal hyphae were seen perforating the wall of the parenchyma cell. The 15N provisioning of the fungus in the galleries resulted in significant enrichment of the 15N signature of the plant's leaves 1 d after the 15N-labelling solution was deposited on the fungus-bearing trap. Finally, NanoSIMS imaging proved that nitrogen was transferred biotrophically from the fungus to the stem tissue. This study provides evidence that the fungi are connected endophytically to an ant-plant system and actively transfer nitrogen from 15N-labelling solution to the plant's stem tissues. Overall, this study underlines how complex the trophic structure of ant-plant interactions is due to the presence of the fungus and provides insight into the possibly important nutritional aspects and tradeoffs involved in myrmecophyte-ant mutualisms.

How species with similar ecological requirements avoid competitive exclusion remains contentious, especially in the species‐rich tropics. Niche differentiation has been proposed as a major mechanism for species coexistence. However, different niche dimensions must be studied simultaneously to assess their combined effects on diversity and composition of a community. In most terrestrial ecosystems, ants are among the most abundant and ubiquitous animals. Since they display direct, aggressive competition and often competitively displace subordinate species from resources, niche differentiation may be especially relevant among ants. We studied temporal and trophic niche differentiation in a ground ant community in a forest fragment in French Guiana. Different baits were presented during day and night to assess the temporal and dietary niches of the local species. They represented natural food resources such as sugars, carrion, excrements, seeds, and live prey. In addition, pitfalls provided a background measure of ant diversity. The communities attracted to the different baits significantly differed from each other, and even less attractive baits yielded additional species. We detected species specialized on living grasshoppers, sucrose, seeds, or dead insects. Community‐level differences between day and night were larger than those between baits, and many species were temporally specialized. In contrast to commonness, foraging efficiency of species was correlated to food specialization. We conclude that many ant species occupy different temporal or dietary niches. However, for many generalized species, the dietary, and temporal niche differentiation brought forward through our sampling effort, cannot alone explain their coexistence.

In Oecophylla, an ant genus comprising two territorially dominant arboreal species, workers are known to (1) use anal spots to mark their territories, (2) drag their gaster along the substrate to deposit short-range recruitment trails, and (3) drag the extruded rectal gland along the substrate to deposit the trails used in long-range recruitment. Here we study an overlooked but important marking behavior in which O. longinoda workers first rub the underside of their mandibles onto the substrate, and then—in a surprising posture—tilt their head and also rub the upper side of their mandibles. We demonstrate that this behavior is used to recruit nestmates. Its frequency varies with the rate at which a new territory, a sugary food source, a prey item, or an alien ant are discovered. Microscopy analyses showed that both the upper side and the underside of the mandibles possess pores linked to secretory glands. So, by rubbing their mandibles onto the substrate, the workers probably spread a secretion from these glands that is involved in nestmate recruitment.

To meet their need for nitrogen in the restricted foraging environment provided by their host plants, some arboreal ants deploy group ambush tactics in order to capture flying and jumping prey that might otherwise escape. Here we show that the ant Allomerus decemarticulatus uses hair from the host plant's stem, which it cuts and binds together with a purpose-grown fungal mycelium, to build a spongy 'galleried' platform for trapping much larger insects. Ants beneath the platform reach through the holes and immobilize the prey, which is then stretched, transported and carved up by a swarm of nestmates. To our knowledge, the collective creation of a trap as a predatory strategy has not been described before in ants.

Fungus-growing attine ants use natural-product antibiotics produced by mutualist actinobacteria as ‘weedkillers’ in their fungal gardens. Here we report for the first time that fungus-growing Allomerus ants, which lie outside the tribe Attini , are associated with antifungal-producing actinobacteria, which offer them protection against non-cultivar fungi isolated from their ant-plants.

The diversity and functional identity of organisms are known to be relevant to the maintenance of ecosystem processes but can be variable in different environments. Particularly, it is uncertain whether ecosystem processes are driven by complementary effects or by dominant groups of species. We investigated how community structure (i.e., the diversity and relative abundance of biological entities) explains the community-level contribution of Neotropical ant communities to different ecosystem processes in different environments. Ants were attracted with food resources representing six ant-mediated ecosystem processes in four environments: ground and vegetation strata in cropland and forest habitats. The exploitation frequencies of the baits were used to calculate the taxonomic and trophic structures of ant communities and their contribution to ecosystem processes considered individually or in combination (i.e., multifunctionality). We then investigated whether community structure variables could predict ecosystem processes and whether such relationships were affected by the environment. We found that forests presented a greater biodiversity and trophic complementarity and lower dominance than croplands, but this did not affect ecosystem processes. In contrast, trophic complementarity was greater on the ground than on vegetation and was followed by greater resource exploitation levels. Although ant participation in ecosystem processes can be predicted by means of trophic-based indices, we found that variations in community structure and performance in ecosystem processes were best explained by environment. We conclude that determining the extent to which the dominance and complementarity of communities affect ecosystem processes in different environments requires a better understanding of resource availability to different species.

This study focuses on species occupying the three strata of an Amazonian rainforest: the ground and leaf litter, the understorey and the canopy. We employed only two sampling techniques: Winkler extraction for ground‐dwelling ants and direct observations for understorey and canopy species on large branches cut off by a climber. We identified 494 ant species from 10 subfamilies and 77 genera over ≈3.0 ha (Chao1 = 607 species; 95% CI: 566–670 species). Although we found fewer arboreal ants compared to approaches using insecticide fogging, this study confirms similarities between the ant diversity in Amazonian and Mesoamerican rainforests. The functional traits of these ants (i.e., diet, nest‐site preference, population size of the colony) allowed us to identify seven clusters. Cluster 1 is a “hodgepodge” grouping arboreal or ground‐dwelling species with different‐sized colonies (76 species). Cluster 2 primarily includes small colonies of ground‐nesting generalist feeders (142 species). Cluster 3 comprises all arboreal species from the understorey inhabiting myrmecophyte domatia or palm trees plus arboreal species with medium‐sized colonies (37 species). Cluster 4 includes all territorially dominant arboreal ants plus one ground‐dwelling species (21 species). All fungus‐growing species belong to Cluster 5, which also contains ground‐nesting generalist feeders and generalist predators (148 species). All doryline army ants are grouped in Cluster 6 along with one ponerine known for its nomadic behavior (15 species). Almost all specialized predators belong to Cluster 7 (55 species); however, Cluster 5 includes two ponerine species that prey exclusively on termites. Based on a nonmetric multidimensional scaling (NMDS), we confirmed that the position of these clusters corresponded fairly well to the three forest strata. Thus, analyzing functional traits enables the trophic position of most ants and their place in the vertical strata of Neotropical rainforests to be determined. We examined the three strata of an Amazonian rainforest (e.g., the ground and leaf litter, understory and canopy) using only two sampling techniques and analyzed their functional traits. We identified 494 ant species from 10 subfamilies and 77 genera over ≈3.0 ha, showing that they are species rich and abundant, particularly at ground level. The functional traits of these ant species based on their diet, nest‐site preference, size of the colony, and the stratum where they live allowed us to identify seven clusters.

Sexual reproduction can lead to major conflicts between sexes and within genomes1, 2, 3, 4. Here we report an extreme case of such conflicts in the little fire ant Wasmannia auropunctata. We found that sterile workers are produced by normal sexual reproduction, whereas daughter queens are invariably clonally produced. Because males usually develop from unfertilized maternal eggs in ants and other haplodiploid species, they normally achieve direct fitness only through diploid female offspring. Hence, although the clonal production of queens increases the queen's relatedness to reproductive daughters, it potentially reduces male reproductive success to zero. In an apparent response to this conflict between sexes, genetic analyses reveal that males reproduce clonally, most likely by eliminating the maternal half of the genome in diploid eggs. As a result, all sons have nuclear genomes identical to those of their father. The obligate clonal production of males and queens from individuals of the same sex effectively results in a complete separation of the male and female gene pools. These findings show that the haplodiploid sex-determination system provides grounds for the evolution of extraordinary genetic systems and new types of sexual conflict

Due to the unbalanced distribution of their fauna and flora, which leads to the creation of a niche opportunities, it is generally accepted that island communities offer weak biotic resistance to biological invasion. In order to empirically test this statement, we compared resource use by ants in the understorey of an undisturbed New Caledonian rain forest recently invaded by the little fire ant, Wasmannia auropunctata. We tested the exploitation of: (1) food sources by placing baits on all trees with trunks greater than 5 cm in diameter; and (2) nesting sites on two tree species likely to shelter ant colonies. In non-invaded areas, the native ants occupied only 44.6% of the baits after 2 h of exposure, while in invaded areas all the baits were occupied by numerous W. auropunctata workers. Similarly, in non-invaded areas only 48.9% of Meryta coriacea (Araliaceae) trees and 64.5% of Basselinia pancheri (Arecaceae) sheltered ants, while in invaded areas W. auropunctata nested in 92.6–98.3% of these trees. Also, workers attended native Margarodidae (Hemiptera) for which they promoted the development of populations significantly larger than those attended by native ants. Thus native ants appear unable to efficiently exploit and defend several of the available food sources and nesting sites, providing a niche opportunity for an invader like W. auropunctata.