Predatory abilities favour the success of the invasive ant Pheidole megacephala in an introduced area

Abstract:  The invasive African big-headed ant, Pheidole megacephala , is a dominant species in the many areas it has invaded. We examined whether one potential reason for its ecological success might be its predatory efficiency. We compared the density of termite nests in an area of Mexico invaded by P. megacephala with an adjacent area where P. megacephala is not present. We also compared the success of P. megacephala in preying on termites with that of 13 native ant species. We found that termite nest density was significantly lower in areas invaded by P. megacephala (0.33 vs. 1.05 nests per 30 m transect). In field trials, we established that P. megacephala workers were significantly more successful at capturing termite workers from termite nest fragments than even the most successful native ant species, Dorymyrmex pyramicus . For both P. megacephala and D. pyramicus , single scouts could trigger the mass recruitment of nestmates, but P. megacephala was able to recruit greater numbers of nestmates. Combined with their aggressiveness towards other ant species, their highly efficient predatory capacities help explain the ecological success of P. megacephala and demonstrate how it can be a major threat to invertebrate biodiversity in the areas it invades.     

Paralyzing action from a distance in an arboreal African ant species

Due to their prowess in interspecific competition and ability to catch a wide range of arthropod prey (mostly termites with which they are engaged in an evolutionary arms race), ants are recognized as a good model for studying the chemicals involved in defensive and predatory behaviors. Ants' wide diversity of nesting habits and relationships with plants and prey types implies that these chemicals are also very diverse. Using the African myrmicine ant Crematogaster striatula as our focal species, we adopted a three-pronged research approach. We studied the aggressive and predatory behaviors of the ant workers, conducted bioassays on the effect of their Dufour gland contents on termites, and analyzed these contents. (1) The workers defend themselves or eliminate termites by orienting their abdominal tip toward the opponent, stinger protruded. The chemicals emitted, apparently volatile, trigger the recruitment of nestmates situated in the vicinity and act without the stinger having to come into direct contact with the opponent. Whereas alien ants competing with C. striatula for sugary food sources are repelled by this behavior and retreat further and further away, termites defend their nest whatever the danger. They face down C. striatula workers and end up by rolling onto their backs, their legs batting the air. (2) The bioassays showed that the toxicity of the Dufour gland contents acts in a time-dependent manner, leading to the irreversible paralysis, and, ultimately, death of the termites. (3) Gas chromatography-mass spectrometry analyses showed that the Dufour gland contains a mixture of mono- or polyunsaturated long-chain derivatives, bearing functional groups like oxo-alcohols or oxo-acetates. Electrospray ionization-mass spectrometry showed the presence of a molecule of 1584 Da that might be a large, acetylated alkaloid capable of splitting into smaller molecules that could be responsible for the final degree of venom toxicity.     

Foraging,recruitment and predation by Decamorium uelense (Sanstchi) (Formicidae: Myrmicinae) on termites in Southern Guinea Savanna,Nigeria

Summary The myrmicine ant Decamorium uelense is a predator of small termites which feed inside their food sources of roots and plant debris. The ant uses a specialized recruitment regime to secure its prey. A scout ant searches for foraging termites and returns to the nest where it recruits a column of 10–30 ants which attack and immobilize the termites. A mass recruitment phase is then instigated, with larger numbers of ants retrieving the prey. The major prey item is Microtermes (consumed at an annual rate of 632 termites m^-2), with other small termites accounting for 0.5% of the total predation. The annual predation of Microtermes in primary savanna woodland by D. uelense removes 74% of the standing population.     

Efficiency in the exploitation of patchy environments by the ponerine antPaltothyreus tarsatus: an ecological consequence of the flexibility of prey capture behavior

Paltothyreus tarsatus workers show an adaptive predatory strategy compatible with central place theory which predicts that single-prey loading is an extension of the optimal diet choice while multiple-prey loading behavior would correspond to the optimal use of patches. The insight learning involved in the quick modifications of predatory strategy enablesP. tarsatus to hunt all available prey in a great diversity of sizes and species. Nevertheless, this generalist predator strongly preferred termites and very large prey such as giant diplopods and crickets to other choices within its diet. In the hunting of these favorite prey, the recruitment of nestmates enhanced the efficiency of total predation, though the release of a chemical trail appeared to depend on the hunger-satiety balance of the colony. In addition to the hunger, the miscapture of prey also triggered the release of chemical trails. The strategy for capturing grouped termites was characterized by the loading of multiple prey at a single time, by a concentrated search in a restricted area and by an optional recruitment of nestmates. These behavioral characteristics of ponerine ants probably account for the flexibility of their predatory strategy for hunting aggregated small prey.     

The predatory behaviour of a tramp ant species in its native range

Workers of the pest ant Paratrechina longicornis participate in a type of group hunting. Each individual forages with its long antennae wide open and moves quickly (6.3 cm/s) along an erratic path surrounded by nestmates behaving in the same way and within range of a recruiting pheromone. They detect prey by contact with successful workers singly capturing and retrieving small prey and seizing larger ones by an appendage. Then they recruit nestmates at short-range; all together they spread-eagle the prey and retrieve them whole.     

The hunting behavior of the African ponerine ant Pachycondyla pachyderma

The hunting behavior of the African ponerine ant Pachycondyla pachyderma, a semi-specialized centipede predator, appears well adapted to this kind of prey and shows a graded complexity according to the difficulty it has in overwhelming prey. Small prey (5-to-8-mm-long termites) were detected by contact and seized by the thorax while larger prey (≥30-mm-long centipedes) were frequently detected from a distance and seized by the anterior-most part of their body. Termites and 30-mm-long lithobiomorph centipedes were not always stung, whereas stinging and even repeated stinging was needed for 50-mm-long geophilomorphs and scolopendromorphs. Moreover, overwhelming wide and heavy scolopendromorphs, which have better defensive abilities, involved the use of additional behaviors allowing the workers to capture them safely: venom spreading, and a peculiar stinging posture, the “fatal embrace”. Here the workers seize scolopendromorphs by an antenna or by one of their first legs, wrap themselves around the prey while maintaining their grip with their mandibles and legs, and slowly inject venom into the prey's ventral surface. Workers retrieve small prey solitarily while, for large geophilomorphs and scolopendromorphs, nestmates can be recruited at short range or even at long range through tandem running.     

An Overlooked Mandibular-Rubbing Behavior Used during Recruitment by the African Weaver Ant,Oecophylla longinoda

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.     

Recruitment Behavior During Foraging in the Neotropical Ant Gnamptogenys moelleri (Formicidae: Ponerinae): Does the Type of Food Matter?

Gnamptogenys moelleri nests in bromeliads and feeds on an array of food items, including dead and live animals, and nectar. Field data in Brazilian forests indicate that G. moelleri hunts solitarily, while retrieving is performed both by solitary workers for small items, or by a group of recruited workers for large items. This flexible foraging strategy was investigated in the laboratory through a series of experiments to assess the context in which recruitment is elicited. Three types of food were used: 50% honey solution, large insect prey, and cluster of small insects. For all food types the first encounter by a scout resulted in increased numbers of ants leaving the nest and finding the food in the arena. After finding liquid food or large prey, the forager returns to the nest and transmits information to nestmates about food location on the substrate. The successful scout repeatedly taps the sting on the ground, and recruited ants collectively retrieve the large insect to the nest. On the other hand, there is no transmission of information to nestmates about the location of small clumped prey, although the returning scout induces nestmates to leave the nest and hunt. Because foraging in G. moelleri is restricted mostly to the nest bromeliad, and small worker size (0.5 cm) precludes capturing large prey solitarily, recruitment behavior widens the spectrum of food items consumed by this ant species. Although recruitment behavior in ponerines has already been reported to vary with the type and size of a food source, this study also shows that the transmission of information about food location depends on the type of food found (large prey or liquid food versus cluster of small prey).     

Predatory behavior of a seed-eating ant:Brachyponera senaarensis

The great flexibility of the feeding strategies exhibited by the ponerine ant Brachyponera senaarensis (Mayr) allows it to exploit either seeds or animal prey items as food resources. Predation is generally limited to small prey and is very similar to scavenging behavior. In laboratory conditions, the predatory behavior of B. senaarensis is not different in structure from that known in other carnivorous ants species. The workers forage individually and return to the nest using a series of cues involving light, a chemical graduated marking system near the nest entrance, and memory. During nest-moving, recruitment by tandem running was observed. However, in colonies where the food supply is regular, workers that discover food do not recruit nestmates, but make repeated trips between the nest and the food source. On the contrary, in starved colonies, the introduction of prey may produce a massive exit of foragers, corresponding to a primitive form of mass recruitment similar to that observed in some other ant species.     

Hunting strategy of a generalist ant species proposed as a biological control agent against termites

We studied the hunting behaviour of Myrmicaria opaciventris (Hymenoptera: Formicidae) in order to evaluate if it can be used as a biological control agent against the termites that damage sugarcane plantations. Hunting workers foraged in groups and recruited nestmates at short-range when they encountered large termite soldiers or groups of small termite workers. Differences in prey capture concerned the: (1) means of detection (from a distance or by contact); (2) termite body part seized (small termites seized by the body; large termites by an appendage); (3) percentages of prey abandoned; and (4) use of venom. The sting of the workers is spatulated implying a topical application of the venom on the prey. Large termites were stretched by several workers whose adherence to the substrate is facilitated by well-developed arolia and claws on the legs while others spread venom on the body and carved it up. An adaptation to termite capture was noted with a distribution of tasks between the workers which subdued prey, and those which transported it. In the former case, the workers easily eliminated termite soldiers, successively attacked several termite workers and even captured new individuals while holding the first ones captured between their mandibles before retrieving them all at once. The remaining individuals were retrieved by the transporting workers. Given this particularly effective predatory strategy, we concluded that, under certain conditions, M. opaciventris can be used as a biological control agent against termites.     

Use of termites, Reticulitermes virginicus, as a springboard in the invasive success of a predatory ant, Pachycondyla (=Brachyponera) chinensis

Invasive ant species have general diet and nest requirements, which facilitate their establishment in novel habitats and their dominance over many native ants. The Asian needle ant, Pachycondyla chinensis, native throughout Australasia was introduced to the southeastern US where it has become established in woodland habitats, nests in close proximity to and consumes subterranean termites (Rhinotermitidae). P. chinensis do not occur in habitats lacking Rhinotermitidae. We suggest that subterranean termites are critical for P. chinensis success in new habitats. We demonstrate that P. chinensis is a general termite feeder, retrieving Reticulitermes virginicus five times more often than other potential prey near P. chinensis colonies. Odors produced by R. virginicus workers, as well as other potential prey, attract P. chinensis. Furthermore, P. chinensis occupy R. virginicus nests in the lab and field and display behaviors that facilitate capture of R. virginicus workers and soldiers. Termites are an abundant, high quality, renewable food supply, in many ways similar to the hemipteran honeydew exploited by most other invasive ant species. We conclude that the behavior of P. chinensis in the presence of termites increases their competitive abilities in natural areas where they have been introduced.     

Cryptic termites avoid predatory ants by eavesdropping on vibrational cues from their footsteps

Eavesdropping has evolved in many predator–prey relationships. Communication signals of social species may be particularly vulnerable to eavesdropping, such as pheromones produced by ants, which are predators of termites. Termites communicate mostly by way of substrate‐borne vibrations, which suggest they may be able to eavesdrop, using two possible mechanisms: ant chemicals or ant vibrations. We observed termites foraging within millimetres of ants in the field, suggesting the evolution of specialised detection behaviours. We found the termite Coptotermes acinaciformis detected their major predator, the ant Iridomyrmex purpureus, through thin wood using only vibrational cues from walking, and not chemical signals. Comparison of 16 termite and ant species found the ants‐walking signals were up to 100 times higher than those of termites. Eavesdropping on passive walking signals explains the predator detection and foraging behaviours in this ancient relationship, which may be applicable to many other predator–prey relationships.     

Behavioral changes in the termite, Coptotermes formosanus (Isoptera), inoculated with six fungal isolates

The studies of pathogen-prevention behaviors of termites have focused on hygiene behavior directed only against highly virulent pathogens. Therefore, we compared behavioral changes in the subterranean termite Coptotermes formosanus following contact with entomopathogenic fungi with different levels of virulence. The fungal virulence was inferred from the daily mortality and the LD₅₀ value in previous data. When untreated termites were allowed to contact their fungus-inoculated nestmates, mutual grooming was frequent during 30 min after inoculation. The inoculated termites were often attacked and eaten by their uninoculated nestmates, and then buried after death. Notably, there was no influence of fungal virulence on these pathogen-prevention behaviors. However, the fungal isolates and genera affected not only the frequency of the behaviors but also the horizontal transmission pattern, the number of dead individuals and the survival period before the first death following infection.     

Regulated food recruitment through individual behavior of scouts in the ant,Myrmica sabuleti (Hymenoptera: Formicidae)

By presenting different kinds of food sources to colonies ofM. sabuleti, we have demonstrated that this species regulates its foraging activity by altering the proportion of scouts that return to the nest to recruit nestmates after discovering a food source and by varying the number of nestmates recruited by a scout. These two parameters are related to the kind of food discovered. Our behavioral experiments showed that the probability that a scout returned to the nest decreased with a decreasing quantity of sucrose solution. In contrast, the number of returned scouts that elicited recruitment from the nest and the mean number of nestmates recruited by one of these scouts were independent of the quantity of the sucrose solution. Recruitment even occurred toward a 1- or 0.25-µl droplet of sucrose solution. When a scout discovered a large dead prey, a large drop of prey juice, a cluster of 30 dead fruit flies, or 1 isolated fruit fly, it always went back to the nest, but it elicited recruitment only when the food source was a large dead prey or a large drop of prey juice. No recruitment occurred when the food source was a single fruit fly and recruitment occurred only once in 30 trials when a cluster of 30 fruit flies was discovered.     

Protein marking reveals predation on termites by the woodland ant, <Emphasis Type="Italic">Aphaenogaster rudis</Emphasis>

Subterranean termites provide a major potential food source for forest-dwelling ants, yet the interactions between ants and termites are seldom investigated largely due to the cryptic nature of both the predator and the prey. We used protein marking (rabbit immunoglobin protein, IgG) and double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) to examine the trophic interactions between the woodland ant, Aphaenogaster rudis (Emery) and the eastern subterranean termite, Reticulitermes flavipes (Kollar). We marked the prey by feeding the termites paper treated with a solution of rabbit immunoglobin protein (IgG). Subsequently, we offered live, IgG-fed termites to ant colonies and monitored the intracolony distribution of IgG-marked prey. Laboratory experiments on the distribution of protein-marked termite prey in colonies of A. rudis revealed that all castes and developmental stages receive termite prey within 24 h. In field experiments, live, protein-marked termites were offered to foraging ants. Following predation, the marker was recovered from the ants, demonstrating that A. rudis preys on R. flavipes under field conditions. Our results provide a unique picture of the trophic-level interactions between predatory ants and subterranean termites. Furthermore, we show that protein markers are highly suitable to track trophic interactions between predators and prey, especially when observing elusive animals with cryptic food-web ecology. Received 19 January 2007; revised 23 March 2007; accepted 26 March 2007.     

Cooperative prey-retrieving in the ant Cataglyphis floricola: an unusual short-distance recruitment

Cataglyphis ants are mostly scavengers adapted to forage individually in arid environments. Although they are widely thought to have lost the capacity of recruitment, we provide evidence that C. floricola foragers that find a large prey near their nest are able to solicit the help of nestmates to carry it cooperatively. After discovering a non-transportable prey, these ants readily return to their nest and stimulate the exit of several recruits. This rudimentary form of recruitment, which is absent in the sympatric species C. rosenhaueri, is only employed when the prey is sufficiently close to the nest entrance (<1 m) and does not allow the food location to be communicated. Instead, C. floricola recruits search for the prey in all directions until they discover it and transport it cooperatively to their nest.     

Recruitment in starved nests: the role of direct and indirect interactions between scouts and nestmates in the ant <Emphasis Type="Italic">Lasius niger</Emphasis>

In social insects, the foraging activity usually increases with the length of food deprivation. In Lasius niger, a mass-recruiting ant species, the foraging adjustment to the level of food deprivation is regulated by the scout that fed at the food source and by the response of the nestmates to signals performed by the scout inside the nest. In this study, we look at the role of these direct interactions (antennations or trophallaxes) and indirect interactions (pheromonal emission) and how they are influenced by the level of food deprivation. At the beginning of recruitment, the relative number of nestmates leaving the nest to forage increases with the level of deprivation. The nestmates’ propensity to exit the nest is not influenced by a previous trophallactic and/or antennal contact with a scout. Our results strongly suggest that the exit of nestmates is triggered by a chemical signal emitted by a scout. Deprivation lowers the response threshold of nestmates to this chemical signal resulting in a more important exit from the nest. Surprisingly, 27% of starved nestmates that receive food from the scout relay the information by depositing a chemical signal before having discovered and drunk the food source. Both phenomena boost the recruitment process. Though successful foragers returning to the nest have a significant role in the recruitment to the food source, we observed that the response of the nestmates inside the nest also greatly influence regulation of the foraging activity.     

Trail Communication During Foraging and Recruitment in the Subterranean Termite Reticulitermes santonensis De Feytaud (Isoptera, Rhinotermitidae)

The search for food in the French subterranean termite Reticulitermes santonensis De Feytaud is organized in part by chemical trails laid with the secretion of their abdominal sternal gland. Trail-laying and -following behavior of R. santonensis was investigated in bioassays. During foraging for food termites walk slowly (on average, 2.3 mm/s) and lay a dotted trail by dabbing the abdomen at intervals on the ground. When food is discovered they return at a quick pace (on average, 8.9 mm/s) to the nest, laying a trail for recruiting nestmates to the food source. While laying this recruitment trail the workers drag the abdomen continuously on the ground. The recruitment trail is highly attractive: it is followed within a few seconds, by more nestmates, and at a quicker pace (on average, 6.4 mm/s) than foraging trails (on average, 2.9 mm/s). The difference between foraging and recruitment trails in R. santonensis could be attributed to different quantities of trail pheromone. A caste-specific difference in trail pheromone thresholds, with workers of R. santonensis being more sensitive to trails than soldiers, was also documented: soldiers respond only to trails with a high concentration of trail pheromone.     

Effects of sublethal exposure to imidacloprid on subsequent behavior of subterranean termite Reticulitermes virginicus (Isoptera: Rhinotermitidae)

Experiments were conducted to determine whether subterranean termites, Reticuliternes virginicus (Banks), previously exposed to sublethal doses of imidacloprid (Premise), and allowed to recover for 1 wk, demonstrated behavioral aversion to a subsequent exposure. Worker termites experiencing a previous sublethal but debilitating exposure to imidacloprid-treated sand (either 10 or 100 ppm for 4 h) showed no apparent aversion to a second encounter with imidacloprid-treated sand under conditions of this experiment. If these laboratory results hold in the field and termites traveling through a zone of soil treated with imidacloprid are impaired but subsequently recover, they will be just as likely as their naive nestmates to reenter the treated area if their travels take them through the nonrepellent application a second time. Our results also indicate that a sublethal exposure to imidacloprid can affect termite tunneling behavior. Many worker termites that received an initial 4-h exposure to 100 ppm imidacloprid-treated sand died, but those that survived tunneled significantly less than did their naive nestmates, as did some termites exposed to 10 ppm imidacloprid.     

Prey capture behavior in an arboreal African ponerine ant

I studied the predatory behavior of Platythyrea conradti, an arboreal ponerine ant, whereas most species in this subfamily are ground-dwelling. The workers, which hunt solitarily only around dusk, are able to capture a wide range of prey, including termites and agile, nocturnal insects as well as diurnal insects that are inactive at that moment of the Nyctemeron, resting on tree branches or under leaves. Prey are captured very rapidly, and the antennal palpation used by ground-dwelling ponerine species is reduced to a simple contact; stinging occurs immediately thereafter. The venom has an instant, violent effect as even large prey (up to 30 times the weight of a worker) never struggled after being stung. Only small prey are not stung. Workers retrieve their prey, even large items, singly. To capture termite workers and soldiers defending their nest entrances, ant workers crouch and fold their antennae backward. In their role as guards, the termites face the crouching ants and end up by rolling onto their backs, their legs batting the air. This is likely due to volatile secretions produced by the ants' mandibular gland. The same behavior is used against competing ants, including territorially-dominant arboreal species that retreat further and further away, so that the P. conradti finally drive them from large, sugary food sources.