Sequential Subterranean Transport of Excavated Sand and Foraged Seeds in Nests of the Harvester Ant,Pogonomyrmex badius

During their approximately annual nest relocations, Florida harvester ants (Pogonomyrmex badius) excavate large and architecturally-distinct subterranean nests. Aspects of this process were studied by planting a harvester ant colony in the field in a soil column composed of layers of 12 different colors of sand. Quantifying the colors of excavated sand dumped on the surface by the ants revealed the progress of nest deepening to 2 m and enlargement to 8 L in volume. Most of the excavation was completed within about 2 weeks, but the nest was doubled in volume after a winter lull. After 7 months, we excavated the nest and mapped its structure, revealing colored sand deposited in non-host colored layers, especially in the upper 30 to 40 cm of the nest. In all, about 2.5% of the excavated sediment was deposited below ground, a fact of importance to sediment dating by optically-stimulated luminescence (OSL). Upward transport of excavated sand is carried out in stages, probably by different groups of ants, through deposition, re-transport, incorporation into the nest walls and floors and remobilization from these. This results in considerable mixing of sand from different depths, as indicated in the multiple sand colors even within single sand pellets brought to the surface. Just as sand is transported upward by stages, incoming seeds are transported downward to seed chambers. Foragers collect seeds and deposit them only in the topmost nest chambers from which a separate group of workers rapidly transports them downward in increments detectable as a "wave" of seeds that eventually ends in the seed chambers, 20 to 80 cm below the surface. The upward and downward transport is an example of task-partitioning in a series-parallel organization of work carried out by a highly redundant work force in which each worker usually completes only part of a multi-step process.     

Nest Enlargement in Leaf-Cutting Ants: Relocated Brood and Fungus Trigger the Excavation of New Chambers

During colony growth, leaf-cutting ants enlarge their nests by excavating tunnels and chambers housing their fungus gardens and brood. Workers are expected to excavate new nest chambers at locations across the soil profile that offer suitable environmental conditions for brood and fungus rearing. It is an open question whether new chambers are excavated in advance, or will emerge around brood or fungus initially relocated to a suitable site in a previously-excavated tunnel. In the laboratory, we investigated the mechanisms underlying the excavation of new nest chambers in the leaf-cutting ant Acromyrmex lundi. Specifically, we asked whether workers relocate brood and fungus to suitable nest locations, and to what extent the relocated items trigger the excavation of a nest chamber and influence its shape. When brood and fungus were exposed to unfavorable environmental conditions, either low temperatures or low humidity, both were relocated, but ants clearly preferred to relocate the brood first. Workers relocated fungus to places containing brood, demonstrating that subsequent fungus relocation spatially follows the brood deposition. In addition, more ants aggregated at sites containing brood. When presented with a choice between two otherwise identical digging sites, but one containing brood, ants'' excavation activity was higher at this site, and the shape of the excavated cavity was more rounded and chamber-like. The presence of fungus also led to the excavation of rounder shapes, with higher excavation activity at the site that also contained brood. We argue that during colony growth, workers preferentially relocate brood to suitable locations along a tunnel, and that relocated brood spatially guides fungus relocation and leads to increased digging activity around them. We suggest that nest chambers are not excavated in advance, but emerge through a self-organized process resulting from the aggregation of workers and their density-dependent digging behavior around the relocated brood and fungus.     

Excavated substrate modulates growth instability during nest building in ants

In social insects, the nests of the same species can show a large difference in size and shape. Despite these large variations, the nests share the same substructures, some appearing during nest growth. In ants, the interplay between nest size and digging activity leads to two successive morphological transitions from circular to branched shapes (budding along the perimeter of the circular cavity and tunnelling of the galleries). Like several other self-organized collective behaviours, this phenomenon, as well as the entire nest-digging process, is thought to be modulated by environmental properties. The present study investigates the effect of excavated substrate on the nest morphogenesis and the morphological transitions by using two materials with different cohesions. Here, we show that the two morphological transitions occur more frequently with a cohesive substrate than with a granular one: 96 per cent of cohesive experiments showed both transitions, whereas only 50 per cent did in granular experiments. We found that transitions and excavation cessation follow area–response thresholds: the shape transitions take place and the digging activity stops when the dug area reaches the corresponding threshold values. The shape transition thresholds are lower with the cohesive substrate and that of stopping digging is independent of nest shape and material. According to simulations, the experimental frequencies of transitions found their origin in the competition between transitions and activity cessation and in the difference between the transition threshold values of each substrate. Our results demonstrate how the substrate properties modulate the collective response and lead to various patterns. Considering the non-specific mechanisms at work, such effects of substrate coarseness have their counterparts in various collective behaviours, generating alternative patterns to colonize and exploit the environment.     

Queue Size Determines the Width of Tunnels in the Formosan Subterranean Termite (Isoptera: Rhinotermitidae)

We present a model of tunnel excavation by termites that requires no pheromone labeling of soil or work sites, but instead relies on tactile interactions and individuals who actively orient their movement. Potential termite excavators moved from the tunnel origin towards the distal end of the tunnel and formed a queue behind those termites at the digging face. Delayed termites excavated soil laterally from the tunnel wall at a position governed by their position in the queue of termites. By examining excavation under artificially induced conditions of longer and shorter queues of termites at the tunnel end, we showed that tunnel width increased with increased queue size and the rate of lateral excavation in a process we termed “digging pressure.”     

Soil Moisture and Excavation Behaviour in the Chaco Leaf-Cutting Ant (Atta vollenweideri): Digging Performance and Prevention of Water Inflow into the Nest

The Chaco leaf-cutting ant Atta vollenweideri is native to the clay-heavy soils of the Gran Chaco region in South America. Because of seasonal floods, colonies are regularly exposed to varying moisture across the soil profile, a factor that not only strongly influences workers'' digging performance during nest building, but also determines the suitability of the soil for the rearing of the colony''s symbiotic fungus. In this study, we investigated the effects of varying soil moisture on behaviours associated with underground nest building in A. vollenweideri. This was done in a series of laboratory experiments using standardised, plastic clay-water mixtures with gravimetric water contents ranging from relatively brittle material to mixtures close to the liquid limit. Our experiments showed that preference and group-level digging rate increased with increasing water content, but then dropped considerably for extremely moist materials. The production of vibrational recruitment signals during digging showed, on the contrary, a slightly negative linear correlation with soil moisture. Workers formed and carried clay pellets at higher rates in moist clay, even at the highest water content tested. Hence, their weak preference and low group-level excavation rate observed for that mixture cannot be explained by any inability to work with the material. More likely, extremely high moistures may indicate locations unsuitable for nest building. To test this hypothesis, we simulated a situation in which workers excavated an upward tunnel below accumulated surface water. The ants stopped digging about 12 mm below the interface soil/water, a behaviour representing a possible adaptation to the threat of water inflow field colonies are exposed to while digging under seasonally flooded soils. Possible roles of soil water in the temporal and spatial pattern of nest growth are discussed.     

Nest architecture of the ant <Emphasis Type="Italic">Formica pallidefulva</Emphasis>: structure,costs and rules of excavation

Summary The architecture of underground ant nests was studied in the ant Formica pallidefulva. These ants build shallow (30–45 cm deep) nests, which consist of more or less vertical shafts that bear chambers. Shafts are modular units of nest growth; nests are enlarged by adding more shafts or extending previously existing ones. The nests are top-heavy, their volume declining exponentially with depth. The total volume of the nest is strongly correlated with the number of worker occupying the nest (R² = 0.87). Some of the rules and templates used by workers for nest construction were determined: (a) chambers are formed in the direction of the tunnels leading up to them, (b) the amount of soil excavated per unit time increases with soil temperature and moisture content. The amount of time and energy required to construct a typical nest were approximated using digging ability parameters determined in the lab. We estimate that if a colony was to move twice a year, it would expend around 20% of its energy intake and at least 6% of its worker time on nest excavation.Received 16 December 2002; revised 10 July 2003; accepted 23 July 2003.     

Dynamics of Nest Excavation and Nest Size Regulation of Lasius niger (Hymenoptera: Formicidae)

The adaptation of nest size to its population is one of the most common processes, but little is known about the dynamics nest-building and -enlarging in social context. Furthermore, the mechanisms involved remain totally ignored. We present here the first results of such dynamics in the context of Lasius niger's nest excavation. We find, with an artificial but standardized method, a strong positive correlation between the number of ants and the final nest volume as well as the digging rate. Both grow almost proportionally to population. When the number of individuals is artificially increased (even slightly) in a nest, its dimension is systematically adjusted in the same way as initial excavation. In this process, digging acts as a negative feedback that controls nest enlargement. Experiments revealed that this negative control is due directly to the volume of the nest as well as the physiological or behavioral modification of ants after digging. Finally, amplification of activity was observed during the enlargement phase, suggesting the possible implication of self-organized processes in the volume control mechanism.     

Cooperative food transport in the Neotropical ant, <Emphasis Type="Italic">Pheidole oxyops</Emphasis>

Cooperation in foraging through information sharing is widespread in social insects and has been much studied. In contrast, cooperative transport of food items by groups of workers is less common and has received comparatively little attention. We investigated collective food retrieval in the Neotropical ant Pheidole oxyops, a ground-nesting species in which minor workers (mean body weight 0.6 mg) collectively transport larger dead insects back to the nest entrance. In total, 29% of items and 78% of total mass is transported collectively. We examined the configurations of ants carrying single experimental food items (weight 119 mg, size 10 × 10 × 1 mm) and found it to be non-random, with twice as many carrying ants at the corners as expected. This arrangement is achieved by preferential joining of corners and leaving of sides by carriers. Corner carrying increased carrying speed by up to 29%. Ants also preferentially carried food items from the front and back, versus the middle.     

Simple rules based on pile slope are used in the self organization of sand pile formation by <Emphasis Type="Italic">Pheidole oxyops</Emphasis> ants

We tested the hypothesis that slope influences where worker ants deposit excavated soil on piles near the nest entrance. We predicted that ants will deposit their load near the top of a pile where the slope changes from upward to downward, to prevent material rolling back towards the entrance. We tested this hypothesis by studying five natural colonies of Pheidole oxyops ants at a field site at S?o Sim?o, Brazil. At this site, each colony was dumping sandy soil excavated from its underground nest in a crescent-shaped pile c. 13 cm from and perpendicular to the nest entrance. Each nest was given an experimental sand pile of symmetrical curved cross section on a plywood platform that could be tilted 15 degrees up or down. From videos, the locations where individual ants dumped their soil loads were measured in relation to the inner (position = 0) and outer (position = 1) edges of the pile. When the platform was tilted down the ants deposited their loads significantly closer to the inner edge (0.458 ± 0.007) than when not tilted (0.530 ± 0.006). When the platform was tilted up the ants deposited their loads significantly further from the inner edge (0.626 ± 0.006) than when not tilted (0.522 ± 0.006). These results support the hypothesis that ants use pile slope in deciding where to dump their load. A similar rule is probably used in other ant species that place excavated soil in steep piles near the nest entrance. Received 5 February 2007; revised 10 June 2007; accepted 9 October 2007.     

The carrying of ants (Cataglyphis bicolor Fab.) by others of the same nest

The carrying of ants from the nest by others of the same species ( Cataglyphis bicolor Fab.) is described. Two types of carrying are distinguished, systematic removal of many adults and larval stages to a new nest, and carrying of individuals, alive or dead, that are dropped at distances up to 35 metres from the nest. The rate of carrying of individual ants from a nest varied from 0–15 per day in a population of foragers estimated as about 200, making 1500–2000 exits per day. Live and dead ants appeared to be treated similarly. Live ants, in the cases examined, went back to the nest. Evidence was obtained by marking ants that carriers were distinct in habits from non-carriers, and also excavated earth from the nest.     

Soil temperature, digging behaviour, and the adaptive value of nest depth in South American species of Acromyrmex leaf-cutting ants

In leaf-cutting ants, workers are expected to excavate the nest at a soil depth that provides suitable temperatures, since the symbiotic fungus cultivated inside nest chambers is highly dependent on temperature for proper growth. We hypothesize that the different nesting habits observed in Acromyrmex leaf-cutting ants in the South American continent, i.e. superficial and subterranean nests, depend on the occurrence, across the soil profile, of the temperature range preferred by workers for digging. To test this hypothesis, we first explored whether the nesting habits in the genus Acromyrmex are correlated with the prevailing soil temperature regimes at the reported nest locations. Second, we experimentally investigated whether Acromyrmex workers engaged in digging use soil temperature as a cue to decide where to excavate the nest. A bibliographic survey of nesting habits of 21 South American Acromyrmex species indicated that nesting habits are correlated with the soil temperature regimes: the warmer the soil at the nesting site, the higher the number of species inhabiting subterranean nests, as compared to superficial nests. For those species showing nesting plasticity, subterranean nests occurred in hot soils, and superficial nests in cold ones. Experimental results indicated that Acromyrmex lundi workers use soil temperature as an orientation cue to decide where to start digging, and respond to rising and falling soil temperatures by moving to alternative digging places, or by stopping digging, respectively. The soil temperature range preferred for digging, between 20°C and maximally 30.6°C, matched the range at which colony growth would be maximized. It is suggested that temperature-sensitive digging guides digging workers towards their preferred range of soil temperature. Workers’ thermopreferences lead to a concentration of digging activity at the soil layers where the preferred range occurs, and therefore, to the construction of superficial nests in cold soils, and subterranean ones in hot soils. The adaptive value of the temperature-related nesting habits, and the temperature-sensitive digging, is further discussed.     

Myrmecochory and short-term seed fate in Rhamnus alaternus: Ant species and seed characteristics

Benefits conferred on plants in ant-mediated seed dispersal mutualisms (myrmecochory) depend on the fate of transported seeds. We studied the effects of elaiosome presence, seed size and seed treatment (with and without passage through a bird's digestive tract) on short-term seed fate in Rhamnus alaternus. In our study, we define short-term seed, or initial, seed fate, as the location where ants release the seeds after ant contact with it. The elaiosomes had the most influence on short-term fate, i.e. whether or not seeds were transported to the nest. The workers usually transported big seeds more often than small ones, but small ants did not transport large seeds. Effect of seed size on transport depended on the ant species and on the treatment of the seed (manual extraction simulating a direct fall from the parent plant vs. bird deposition corresponding to preliminary primary dispersal). Probability of removal of elaiosome-bearing seeds to the nest by Aphaenogaster senilis increased with increasing seed weight.     

Excavation and architecture of Argentine ant nests

We used x-ray computed tomography to study the elaboration of nest structures in small sand-filled nest boxes by Argentine ant (Linepithema humile) colonies composed of 10, 100, and 1000 workers. The pattern of nest growth was consistent with a process of density-dependent stimulation of excavation, which subsided as nests grew and the density of digging stimuli declined. Thus, nest excavation would be auto-regulating, and final nest size should be adjusted to colony size. We found that excavation rates and final nest sizes increased with colony size, but were not tenfold greater in 1000-worker colonies than in 100-worker colonies. In the largest colonies, the internal surface area scaled allometrically with volume, so that more surface was obtained relative to volume excavated as the nest grew. Although the gross features of Argentine ant nests, such as total size, seem explicable by a simple, self-organized regulatory process, other features of the nest architecture will require further investigation. Received 3 March 2005; revised 26 April 2005; accepted 3 May 2005.     

Cutters,carriers and transport chains: Distance-dependent foraging strategies in the grass-cutting ant <Emphasis Type="Italic">Atta vollenweideri</Emphasis>

Summary Most studies on leaf-cutting ant foraging examined forest species that harvest dicot leaves. We investigated division of labor and task partitioning during foraging in the grass-cutting ant Atta vollenweideri. Workers of this species harvest grass fragments and transport them to the nest for distances up to 150 m along well-established trunk trails. We recorded the behavior of foraging ants while cutting and monitored the transport of individually-marked fragments from the cutting site until they reached the nest. A. vollenweideri foragers showed division of labor between cutting and carrying, with larger workers cutting the fragments, and smaller ones transporting them. This division was less marked when plants were located very close to the nest and no physical trail was present, i.e., the cutter often transported its own fragment back to the nest. On long foraging trails, the transport of fragments was a partitioned task, i.e., workers formed transport chains composed of 2 to 5 carriers. This sequential load transport occurred more often on long than on short trails. The first carriers in a transport chain covered only short distances before dropping their fragments, and they were observed to turn back and revisit the patch. The last carriers covered the longest distance. The probability of dropping the carried fragment on the trail was independent of both worker and fragment size, and there was no particular location on the trail for dropping, i.e., fragments were not cached. Transport time of fragments transported by a chain was longer than for those transported by single workers all the way to the nest, i.e., sequential transport did not save foraging time. Two hypotheses concerning the possible adaptive value of transport chains are discussed. The first one argues that sequential transport may lead to an increased material transport rate compared to individual transport. The second one considers sequential transport as a way to enhance the information flow among foragers, thus leading to a quicker build-up of workers at particular harvesting places. It is suggested that rather than increasing the gross transport rate of material, transport via chains may favor the transfer of information about the kind of resource being actually harvested.Received 19 December 2002; revised 14 March 2003; accepted 19 March 2003     

Florida Harvester Ant Nest Architecture,Nest Relocation and Soil Carbon Dioxide Gradients

Colonies of the Florida harvester ant, Pogonomyrmex badius, excavate species-typical subterranean nests up the 3 m deep with characteristic vertical distribution of chamber area/shape, spacing between levels and vertical arrangement of the ants by age and brood stage. Colonies excavate and occupy a new nest about once a year, and doing so requires that they have information about the depth below ground. Careful excavation and mapping of vacated and new nests revealed that there was no significant difference between the old and new nests in any measure of nest size, shape or arrangement. Colonies essentially built a replicate of the just-vacated nest (although details differed), and they did so in less than a week. The reason for nest relocation is not apparent. Tschinkel noted that the vertical distribution of chamber area, worker age and brood type was strongly correlated to the soil carbon dioxide gradient, and proposed that this gradient serves as a template for nest excavation and vertical distribution. To test this hypothesis, the carbon dioxide gradient of colonies that were just beginning to excavate a new nest was eliminated by boring 6 vent holes around the forming nest, allowing the soil CO₂ to diffuse into the atmosphere and eliminating the gradient. Sadly, neither the nest architecture nor the vertical ant distribution of vented nests differed from either unvented control or from their own vacated nest. In a stronger test, workers excavated a new nest under a reversed carbon dioxide gradient (high concentration near the surface, low below). Even under these conditions, the new and old nests did not differ significantly, showing that the soil carbon dioxide gradient does not serve as a template for nest construction or vertical worker distribution. The possible importance of soil CO₂ gradients for soil-dwelling animals is discussed.     

Biomantling and Bioturbation by Colonies of the Florida Harvester Ant,Pogonomyrmex badius

In much of the world, soil-nesting ants are among the leading agents of biomantling and bioturbation, depositing excavated soil on the surface or in underground chambers. Colonies of the Florida harvester ant, Pogonomyrmex badius excavate a new nest once a year on average, depositing 0.1 to 12 L (3 L average) of soil on the surface. Repeated surveys of a population of about 400 colonies yielded the frequency of moves (approximately once per year), the distance moved (mean 4 m), and the direction moved (random). The area of the soil disc correlated well with the volume and maximum depth of the nest, as determined by excavation and mapping of chambers. The population-wide frequency distribution of disc areas thus yielded the frequency distribution of nest volumes and maximum depths. For each surveyed colony, the volume of soil excavated from six specified depth ranges and deposited on the surface was estimated. These parameters were used in a simulation to estimate the amount of soil mantled over time by the observed population of P. badius colonies. Spread evenly, P. badius mantling would create a soil layer averaging 0.43 cm thick in a millennium, with 10–15% of the soil deriving from depths greater than 1 m. Biomantling by P. badius is discussed in the context of the ant community of which it is a part, and in relation to literature reports of ant biomantling.     

Quorum sensing by encounter rates in the ant Temnothorax albipennis

Emigrating colonies of the ant Temnothorax (formerly Leptothorax)albipennis can choose the best of several nest sites, even whenthe active ants organizing the move do not compare sites. Thiscollective ability depends on a quorum rule used by ants assessinga candidate site. Only when the site's population has surpasseda threshold do they switch from slow recruitment of fellow activeants by tandem runs to rapid transport of the majority of thecolony. Here, I show that ants perceive the achievement of aquorum through their rate of direct encounters with nest matesat the site. When ants in a crowded site were prevented fromtactile contact with nest mates, they recruited by tandem runs,as though to an empty nest. Furthermore, when the encounterrate was raised independent of population, by reducing the sizeof the candidate nest, ants started to transport at a significantlylower population. The switch occurred at the same encounterrate regardless of nest size, whether the rate was measuredas the mean over the entire visit or as the inverse of the latencyuntil the first encounter. Because encounter rate reflects thedensity of nest mates and thus varies with nest size as wellas population, the ants' collective decision-making algorithmmay be robust to the exact population at which the switch totransport occurs. Ants cease monitoring quorum presence afterswitching to transport, coincident with an abrupt shorteningof visit duration by approximately 2 min, which may be interpretedas the time required for quorum detection.     

Task partitioning in leafcutting ants

A task is said to be partitioned when it is split into two or more sequential stages and material is passed from one worker to another; for instance, one individual collects a material from a source and passes it to another for transportation back to the nest. In this study, we review the existence of task partitioning in leafcutting ants (Attini) and find that, across species, this form of work organisation occurs in all stages of leaf collection, leaf transportation, and leaf processing within the nest; in the deposition of refuse (leaves and spent fungal garden) to internal or external dumps; and in colony emigration. Thus, task partitioning is shown to be a very important component of work organisation in leafcutting ants. Examples mostly concern Atta but task partitioning is also known in Acromyrmex. The costs and benefits of task partitioning of the various stages are discussed and suggestions for further research are highlighted. Electronic Publication     

The Role of Colony Size on Tunnel Branching Morphogenesis in Ant Nests

Many ant species excavate nests that are made up of chambers and interconnecting tunnels. There is a general trend of an increase in nest complexity with increasing population size. This complexity reflects a higher ramification and anastomosis of tunnels that can be estimated by the meshedness coefficient of the tunnelling networks. It has long been observed that meshedness increases with colony size within and across species, but no explanation has been provided so far. Since colony size is a strong factor controlling collective digging, a high value of the meshedness could simply be a side effect of a larger number of workers. To test this hypothesis, we study the digging dynamics in different group size of ants Messor sancta. We build a model of collective digging that is calibrated from the experimental data. Model''s predictions successfully reproduce the topological properties of tunnelling networks observed in experiments, including the increase of the meshedness with group size. We then use the model to investigate situations in which collective digging progresses outward from a centre corresponding to the way tunnelling behaviour occurs in field conditions. Our model predicts that, when all other parameters are kept constant, an increase of the number of workers leads to a higher value of the meshedness and a transition from tree-like structures to highly meshed networks. Therefore we conclude that colony size is a key factor determining tunnelling network complexity in ant colonies.     

Sand Pile Formation in <Emphasis Type="Italic">Dorymyrmex</Emphasis> Ants

We studied circular sand pile formation by two colonies of Brazilian Dorymyrmex ants, in which workers dumped sand excavated from their underground nest around the nest entrance hole. In most cases a worker dumped its load just beyond the ridge of the pile. Each dumped piece either stayed where it was deposited (81.9% in colony A and 73.0% in colony B) or rolled down the outer slope of the sand pile away from the entrance (17.9% in colony A and 27.0% in colony B). Ants almost never dumped in a way that resulted in the load rolling back to the entrance. When one side of the sand pile was experimentally removed, ants preferentially dumped soil on the now flat side, thereby restoring the original circular shape.