Diel pattern driven by free convection controls leaf-cutter ant nest ventilation and greenhouse gas emissions in a Neotropical rain forest

Leaf-cutter ant nests are biogeochemical hot spots where ants live and import vegetation to grow fungus. Metabolic activity and (in wet tropical forests) soil gas flux to the nest may result in high nest CO2 concentrations if not adequately ventilated. Wind-driven ventilation mitigates high CO2 concentrations in grasslands, but little is known about exchange for forest species faced with prolonged windless conditions. We studied Atta cephalotes nests located under dense canopy (leaf area index > 5) in a wet tropical rainforest in Costa Rica, where wind events are infrequent. We instrumented nests with thermocouples and flow-through CO2 sensing chambers. The results showed that CO2 concentrations exiting leaf-cutter ant nests follow a diel pattern with higher values at night. We developed an efflux model based on pressure differences that evaluated the observed CO2 diel pattern in terms of ventilation by (1) free convection (warm, less dense air rises out the nest more prominently at night) and (2) episodic wind-forced convection events providing occasional supplemental ventilation during daytime. Average greenhouse gas emissions were estimated through nest vents at about 78 kg CO2eq nest−1 year−1. At the ecosystem level, leaf-cutter ant nest vents accounted for 0.2% to 1% of total rainforest soil emissions. In wet, clayey tropical soils, leaf-cutter ant nests act as free convection-driven conduits for exporting CO2 and other greenhouse gases produced within the nest (fungus and ant respiration, refuse decay), and by roots and soil microbes surrounding the nest. This allows A. cephalotes nests to be ventilated without reliable wind conditions.     

Size matters: nest colonization patterns for twig‐nesting ants

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Colony Budding and its Effects on Food Allocation in the Highly Polygynous Ant, Monomorium pharaonis

To advance our understanding of the causes and the consequences of budding (colony multiplication by fragmentation of main nests), we investigated nest movement in the facultatively polydomous Pharaoh ant, Monomorium pharaonis. Demographic data revealed that Pharaoh ants are highly polygynous and have a relatively low worker to queen ratio of 12.86. Budding experiments demonstrated that the number of available bud nests has a significant effect on colony fragmentation and increasing the number of bud nests resulted in smaller colony fragments. The overall distribution among bud nests was uneven, even though there was no evidence that the different life stages and castes partitioned unevenly among the bud nests and the analysis of individual colonies revealed no evidence of an uneven split in any of the colonies. This demonstrates that Pharaoh ants have the ability to exert social control over colony size and caste proportions during budding, which may contribute to their success as an invasive ant. The intensity of nest disturbance had a significant effect on whether or not the ants migrated into bud nests. Major disturbance resulted in the ants abandoning the source nest and migrating to bud nests and minor disturbance did not stimulate the ants to abandon the source nest. The results of the successive budding experiment which allowed the ants the opportunity to bud into progressively smaller nest fragments demonstrate that Pharaoh ants maintain a preferred minimum group size of 469 ± 28 individuals. Food allocation experiments utilizing protein marking revealed that nest fragmentation in Pharaoh ants has no negative impact on intracolony food distribution. Overall, our results suggest that nest units in the Pharaoh ant behave like cooperative, rather than competitive, entities. Such cooperation is most likely facilitated by the fact that individuals in all bud nests are genetically related, remain in close proximity to each other, and may continue to exchange individuals after budding.     

Ant Colonies Prefer Infected over Uninfected Nest Sites

During colony relocation, the selection of a new nest involves exploration and assessment of potential sites followed by colony movement on the basis of a collective decision making process. Hygiene and pathogen load of the potential nest sites are factors worker scouts might evaluate, given the high risk of epidemics in group-living animals. Choosing nest sites free of pathogens is hypothesized to be highly efficient in invasive ants as each of their introduced populations is often an open network of nests exchanging individuals (unicolonial) with frequent relocation into new nest sites and low genetic diversity, likely making these species particularly vulnerable to parasites and diseases. We investigated the nest site preference of the invasive pharaoh ant, Monomorium pharaonis, through binary choice tests between three nest types: nests containing dead nestmates overgrown with sporulating mycelium of the entomopathogenic fungus Metarhizium brunneum (infected nests), nests containing nestmates killed by freezing (uninfected nests), and empty nests. In contrast to the expectation pharaoh ant colonies preferentially (84%) moved into the infected nest when presented with the choice of an infected and an uninfected nest. The ants had an intermediate preference for empty nests. Pharaoh ants display an overall preference for infected nests during colony relocation. While we cannot rule out that the ants are actually manipulated by the pathogen, we propose that this preference might be an adaptive strategy by the host to “immunize” the colony against future exposure to the same pathogenic fungus.     

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.     

Hypoxic conditions and oxygen supply in nests of the mangrove ant, Camponotus anderseni, during and after inundation

The small ant Camponotus anderseni lives exclusively in twigs of the mangrove tree Sonneratia alba, and during inundation, the entrance hole is blocked with a soldier’s head which effectively prevents flooding. The nests can be very crowded, with the ants and coccids filling up to 50% of the volume, and due to their metabolic activity, the conditions in the nests during inundation become hypercapnic and hypoxic. Each nest has only one entrance, and the opening is quite small (1.56 ± 0.03 mm). The mean diameter of the galleries is 2.31 ± 0.23 mm, independent of the thickness of the twig and length of the nest. During normal conditions with open nests, the oxygen depletion is substantial in the part of the nest most distant from the opening, and in a 120 mm long nest the oxygen concentration can be as low as 15.7%. During simulated inundation, in which the nest entrances were blocked, the oxygen concentration dropped to very low levels (<0.5%) after one hour. After opening the nest entrance, the oxygen concentration increased again, but for a 100 mm long nest it took nearly 20 minutes before the concentration was back to the normal depressed level. Mathematical modelling of the steady-state oxygen concentrations in the innermost part of the nests shows a lower O₂ concentration than calculated. The time for equilibration of oxygen after inundation is longer than expected for small nests, presumably because the passive diffusion is obstructed by the nest contents. The “dilemma” faced by C. anderseni is to avoid drowning without suffering anoxia or hypercapnia, and they show a remarkable ability to adapt to the extreme conditions in the mangrove and exploit a niche where the density of other ants is insignificant. Received 13 December 2007; revised 30 July 2008; accepted 6 September 2008.     

Estimating density of ant nests using distance sampling

The quantification of ant nest densities is a useful but challenging task given the group’s high abundance and diversity of nesting sites. We present a new application of a distance-sampling method which follows standard distance analytical procedures, but introduces a sampling innovation that is particularly useful for ants; instead of having an observer look for ants we let ants find a bait station and measure the distances covered between nest and station. We test this method by estimating the density of epigaeic ant nests in an Amazon tropical forest site near Manaus, Brazil. We distributed 220 baits of canned sardine mixed with cassava flour among 10, 210-m long transects in old-growth upland forest. Forty-five minutes after baiting, we followed the ants’ trails and measured the linear distance between the bait and each nest’s entrance. We then used the freely available program DISTANCE to estimate the number of nests per unit area while accounting for the effect of distance on the probability that a colony will find a bait. There were found 38 species nesting in 287 different colonies, with an estimated 2.66 nests/m². This estimate fell within the 95 % confidence bounds of nest density predicted for a similar number of species based on a literature survey of ant species richness and nest density. Our sampling solution, however, takes less than 30 % of the time used by conventional sampling approaches for a similar area, with the advantage that it produces not only a point estimate but also a quantification of uncertainty about density.     

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.     

Immigration and formation of mixed colonies in red wood ants (Hymenoptera,Formicidae)

Long-term field studies of the composition and spatial structure of settlements of ants of the Formica rufa group were carried out in two regions of Russia (Moscow and Arkhangelsk provinces). Fragmentation of damaged nests followed by reintegration of the fragments is the main way of formation of mixed colonies of ants from different nests (including different species). The principal factor of nest fragmentation is their damage by wild boars, bears, and in some localities, by poachers. The formation of mixed nests and nest complexes with participation of different Formica species was observed. They are formed by joining the ants from several damaged nests or by a colony from a destroyed nest immigrating into an intact one. Regular damage of many nests leads to the formation of broad zones of mixed colonies. The mixed colonies including 2–3 species of wood ants have recently become common. The phenomenon of mixed colonies raises a question as to the relative importance of two basic principles (sociality and specific identity) in the life of ant societies and demonstrates the priority of the social principle.     

Ants under crowded conditions consume more energy

Social insects live in colonies consisting of many workers, where worker interactions play an important role in regulating colony activities. Workers interact within the social space of the nest; therefore, constraints on nest space may alter worker behaviour and affect colony activities and energetics. Here we show in the ant Temnothorax rugatulus that changes in nest space have a significant effect on colony energetics. Colonies with restricted nest space showed a 14.2 per cent increase in metabolic rate when compared with the same colonies in large uncrowded nests. Our study highlights the importance of social space and shows that constraints on social space can significantly affect colony behaviour and energy use in ants. We discuss the implications of our findings regarding social insects in general.     

Ants move to improve: colonies of Leptothorax albipennis emigrate whenever they find a superior nest site

A high-quality home can be a major factor determining fitness. However, when house hunting becomes necessary, animals might often face a speed-versus-accuracy trade-off and therefore be unable to survey their environment extensively for the optimum site. We found that the ant Leptothorax albipennis was able to correct errors made in such a hurried decision by continuing to survey even after a colony had settled in a nest site. Colonies moved from intact undisturbed nests to another nest site whenever the new nest site presented a sufficient improvement in nest quality. Thus, scout ants must be able to judge and compare the quality of the new, empty nest site with the one currently inhabited by the colony. Emigrations from intact nests were initiated by high numbers of ants recruited by tandem runs. This evidence may explain how a small number of scouts can motivate an entire colony to move when there is no immediate need to do so. Compared with their behaviour in emigrations from destroyed nests, the ants favoured even more strongly accuracy over speed, because they waited for a larger number of scouts to agree on one site before starting the emigration. They could do this without increased risk because the rest of the colony remained safely in the old nest.     

The Antsy Social Network: Determinants of Nest Structure and Arrangement in Asian Weaver Ants

Asian weaver ants (Oecophylla smaragdina) are arboreal ants that are known to form mutualistic complexes with their host trees. They are eusocial ants that build elaborate nests in the canopy in tropical areas. A colony comprises of multiple nests, usually on multiple trees, and the boundaries of the colony may be difficult to identify. However, they provide the ideal model for studying group living in invertebrates since there are a definite number of nests for a given substrate, the tree. Here, we briefly examine the structure of the nests and the processes involved in the construction and maintenance of these nests. We have described the spatial arrangement of weaver ant nests on trees in two distinct tropical clusters, a few hundred kilometres apart in India. Measurements were made for 13 trees with a total of 71 nests in the two field sites. We have considered a host of biotic and abiotic factors that may be crucial in determining the location of the nesting site by Asian weaver ants. Our results indicate that tree characteristics and architecture followed by leaf features help determine nest location in Asian weaver ants. While environmental factors may not be as influential to nest arrangement, they seem to be important determinants of nest structure. The parameters that may be considered in establishing the nests could be crucial in picking the evolutionary drivers for colonial living in social organisms.     

Nest Defense and Conspecific Enemy Recognition in the Desert Ant Cataglyphis fortis

This study focuses on different factors affecting the level of aggression in the desert ant Cataglyphis fortis. We found that the readiness to fight against conspecific ants was high in ants captured close to the nest entrance (0- and 1-m distances). At a 5-m distance from the nest entrance the level of aggression was significantly lower. As the mean foraging range in desert ants by far exceeds this distance, the present account clearly shows that in C. fortis aggressive behavior is displayed in the context of nest, rather than food-territory defense. In addition, ants were more aggressive against members of a colony with which they had recently exchanged aggressive encounters than against members of a yet unknown colony. This finding is discussed in terms of a learned, enemy-specific label-template recognition process.     

The Relationship between Canopy Cover and Colony Size of the Wood Ant Formica lugubris - Implications for the Thermal Effects on a Keystone Ant Species

Climate change may affect ecosystems and biodiversity through the impacts of rising temperature on species’ body size. In terms of physiology and genetics, the colony is the unit of selection for ants so colony size can be considered the body size of a colony. For polydomous ant species, a colony is spread across several nests. This study aims to clarify how climate change may influence an ecologically significant ant species group by investigating thermal effects on wood ant colony size. The strong link between canopy cover and the local temperatures of wood ant’s nesting location provides a feasible approach for our study. Our results showed that nests were larger in shadier areas where the thermal environment was colder and more stable compared to open areas. Colonies (sum of nests in a polydomous colony) also tended to be larger in shadier areas than in open areas. In addition to temperature, our results supported that food resource availability may be an additional factor mediating the relationship between canopy cover and nest size. The effects of canopy cover on total colony size may act at the nest level because of the positive relationship between total colony size and mean nest size, rather than at the colony level due to lack of link between canopy cover and number of nests per colony. Causal relationships between the environment and the life-history characteristics may suggest possible future impacts of climate change on these species.     

鼎突多刺蚁的营巢习性

1985—1986年在浙江永康县城东南10公里的山坡上观察鼎突多刺蚁(Polyrhachis vicina Roger)的营巢习性;见到蚁巢大多分布于山脚附近、温暖而阳光充足的南坡,一般生活于地面,以刺芒野古草(Arundinella setosaTrin.)为主的禾本科草丛中.蚁巢由工蚁使幼虫吐丝把植物残体、昆虫尸体、泥沙和碎石等物缀织而成.地下部分的深度常受气温的影响:5—10月,气温较高,巢深2—4cm、11—4月,气候寒冷,深度可达10—20cm.每个蚁巢内的所有个体为一相对独立的群体,相邻蚁巢的群体间常相互联系、交换幼期个体和食物等.群体常因季节的变化而有迁移现象:秋季至春季,蚁巢大多位于阳光充足的草地上,夏天,由于气候炎热,蚁巢自草地移向遮荫度较大的树林.8—9月,部分上树筑巢.1—8月,蚁巢数不变,8月以后,蚁巢数开始增加,到10月达到最大,以后又下降,到12月降至通常水平.由此可见,9—10月,蚂蚁分巢,11—12月,部分蚁巢又合并.平均每巢工蚁数夏季最多,其次是春季和冬季,秋季由于分巢而最少.     

Experiments with artificial nests provide evidence for ant community stratification and nest site limitation in a tropical forest

Ants are dominant in tropical forests and many species nest in hollow cavities. The manner in which species are vertically stratified in these complex habitats is not known, with lack of nest sites being proposed to limit ant populations. Here, we assess ant community stratification and nest site limitation in a lowland rainforest in New Guinea using experimental addition of artificial bamboo nests of two cavity sizes (small: ~12 mm large: ~32 mm diameter) placed at ground level, in the understorey, and in the canopy. We also conducted a pilot experiment to test the utility of nest translocation. Nests were checked for occupancy after 10 weeks and half of the occupied nests were then translocated between forest plots, while keeping same vertical position. Occupancy of small nests was much higher in the understorey and canopy than at ground level (~75% vs. ~25%). Translocation was successful, as a majority of nests was inhabited by the same species before and after translocation and there was no impact of translocation to a different plot compared to the control, except for a reduction in colony size at ground level. Our experiment demonstrates a vertical stratification in community composition of ants nesting in hollow dead cavities and shows that these ants are more nest site limited in the higher strata than at ground level. Use of small artificial cavities has great potential for future experimental studies, especially for those focused on arboreal ants, as occupancy is high and translocation does not negatively affect their colony size. Abstract in Tok Pisin is available with online material.     

Serial monodomy in ants: an antipredator strategy?

Abstract.  1. The term serial monodomy is used to describe a life-history phenomenon in social insects. Serially monodomous colonies maintain multiple nests for their exclusive use, but only occupy one nest at a time.
2. The hypothesis that colony odours mediate nest relocation decisions was tested in the serially monodomous species Aphaenogaster araneoides from Central America. Odour extracts of colony members were created using a non-polar solvent.
3. Colonies strongly avoided reoccupying nests treated with colony odour extracts, while control colonies often returned to nests subjected to solvent-only control. Behavioural observations indicated that A. araneoides colonies are capable of detecting army ant ( Eciton burchellii ) raids up to 1.4 m from the raiding front, with several seconds to evacuate nests.
4. It is proposed that the function of serial monodomy in A. araneoides is the reduction of nest odour to enhance detection of predaceous army ants. Serial monodomy may be a widespread but undocumented mode of nesting where army ants occur in tropical and subtropical climates.     

Adult transport in the ant Cataglyphis iberica: a means to maintain a uniform colonial odour in a species with multiple nests

Abstract. . Societies of the ant Cataglyphis iberica (Hymenoptera, Formicidae) comprise several satellite queenless nests around a queenright nest. During spring, at the end of hibernation, the incidence of adult transport between these nests is high, but it decreases during summer. Quantitative analyses of the contents of postpharyngeal glands of transporter and transportee ants reveal the amounts of hydrocarbons to be lower in the latter, indicating that these ants are generally younger. Moreover, the more diverse composition of the transportees' secretion may reflect their individual makeup. Transporters, in contrast, maintained a uniform colony odour uirough trophallactic exchanges before entering hibernation. The odour disparity between the transportees and the general colony odour may stimulate the transporters to bear them to the nest containing the queen where they can obtain the colony odour via trophallaxis. The intense traffic between satellite nests in the spring may thus be the means by which a uniform colonial odour is regained after hibernation. Adult transport seems also to be necessary since the young transportee ants are not able to orient themselves and find the other nests.     

Ants on the Move: Resource Limitation of a Litter‐nesting Ant Community in Costa Rica1

The leaf litter of tropical wet forests is replete with itinerant ant nests. Nest movement may help ants evade the constraints of stress and disturbance and increase access to resources. I studied how nest relocation and environmental factors may explain the density, size, and growth of leaf litter ant nests. I decoupled the relationships among litter depth, food abundance, and nest availability in a 4‐mo manipulation of food and leaf litter in a community of litter‐nesting ants in a lowland wet forest in Costa Rica. Over 4 mo, 290 1 m² treatment and control plots were sampled without replacement. Nest densities doubled in response to food supplementation, but did not decrease in response to litter removal or stress (from litter trampling). The supplementation of food increased the utilization of less favored nesting materials. In response to food supplementation and litter trampling, arboreal ants established nests in the litter, and growth rates of the most common ants (Pheidole spp.) increased. Colony growth was independent of colony size and growth rates of the most abundant ants. In general, I conclude that litter‐nesting ant density is driven primarily by food limitation, that nest relocation behavior significantly affects access to resource and the demographic structure of this community, and that nest fission may be a method to break the growth–reproduction trade‐off.     

Driver Ants Invading a Termite Nest: Why Do the Most Catholic Predators of All Seldom Take This Abundant Prey?

Driver ants ( i.e. , epigaeic species in the army ant genus Dorylus , subgenus Anomma ) are among the most extreme polyphagous predators, but termites appear to be conspicuously absent from their prey spectrum and attacks by driver ants on termite nests have not yet been described. Here, we report a Dorylus ( Anomma ) rubellus attack on a colony of the fungus-growing termite Macrotermes subhyalinus that was observed during the dry season in a savannah habitat in Nigeria's Gashaka National Park. It was estimated that several hundred thousand termites (probably more than 2.4 kg dry mass) were retrieved. The apparent rarity of driver ant predation on Macrotermes nests may be explained by different habitat requirements, by the fact that these ants mostly forage aboveground, by efficient termite defense behavior and nest architecture that make entry into the nest difficult, and finally by driver ant worker morphology, which differs remarkably from that of subterranean Dorylus species that regularly invade and destroy termite colonies.