Colony demographics shape nest construction in ants

Curation statements for this article:
  • Curated by eLife

    eLife logo

    eLife Assessment

    This study presents an important finding that ant nest structure and digging behavior depend on ant age demographics for a ground-dwelling ant species (Camponotus fellah). By asking whether ants employ age-polyethism in excavation, the authors address a long-standing question about how individuals in collectives determine the overall state of the task they must perform, and their results may prove to be a key consideration for interpreting results from other studies in the field of social insect behavior. While the experimental evidence that the age of the ants and the group composition affect the digging of tunnels is solid, some of the analyses and modeling are seem superfluous, as they do not further support the results or contribute to a deeper understanding of the system.

This article has been Reviewed by the following groups

Read the full article See related articles

Abstract

The ant nest serves as the skeleton of the ant superorganism. Similar to a skeleton, the nest expands as the colony grows and requires repair after catastrophic events. We experimentally compared nest excavation by colonies seeded from a single mated queen and then allowed to grow for six months, to excavation triggered by a catastrophic event in colonies with fixed demographics. The areas excavated by equal group sizes differed significantly between these conditions: heterogeneous populations in naturally growing colonies as well as cohorts of young ants dig larger areas than old ant cohorts. Moreover, we find that younger ants tend to dig slanted tunnels while older ants dig straight down. This is a novel form of age polyethism, where an ant's age dictates not only her likelihood to engage in a task but also the way she performs the task. We further present a quantitative model that predicts that under normal growth, digging is predominantly performed by the younger ants while after a catastrophe all ants dig to restore lost nest volume. The fact that the nests of naturally growing colonies exhibit slanted tunnels strengthens this prediction. Finally, our results indicate how a colony's demographic and physical history are sketched into the current structure of its nest.

Article activity feed

  1. eLife Assessment

    This study presents an important finding that ant nest structure and digging behavior depend on ant age demographics for a ground-dwelling ant species (Camponotus fellah). By asking whether ants employ age-polyethism in excavation, the authors address a long-standing question about how individuals in collectives determine the overall state of the task they must perform, and their results may prove to be a key consideration for interpreting results from other studies in the field of social insect behavior. While the experimental evidence that the age of the ants and the group composition affect the digging of tunnels is solid, some of the analyses and modeling are seem superfluous, as they do not further support the results or contribute to a deeper understanding of the system.

  2. Reviewer #1 (Public review):

    This study investigates how ant group demographics influence nest structures and group behaviors of Camponotus fellah ants, a ground-dwelling carpenter ant species (found locally in Israel) that build subterranean nest structures. Using a quasi-2D cell filled with artificial sand, the authors perform two complementary sets of experiments to try to link group behavior and nest structure: first, the authors place a mated queen and several pupae into their cell and observe the structures that emerge both before and after the pupae eclose (i.e., "colony maturation" experiments); second, the authors create small groups (of 5,10, or 15 ants, each including a queen) within a narrow age range (i.e., "fixed demographic" experiments) to explore the dependence of age on construction. Some of the fixed demographic instantiations included a manually induced catastrophic collapse event; the authors then compared emergency repair behavior to natural nest creation. Finally, the authors introduce a modified logistic growth model to describe the time-dependent nest area. The modification introduces parameters that allow for age-dependent behavior, and the authors use their fixed demographic experiments to set these parameters, and then apply the model to interpret the behavior of the colony maturation experiments. The main results of this paper are that for natural nest construction, nest areas, and morphologies depend on the age demographics of ants in the experiments: younger ants create larger nests and angled tunnels, while older ants tend to dig less and build predominantly vertical tunnels; in contrast, emergency response seems to elicit digging in ants of all ages to repair the nest.

  3. Reviewer #2 (Public review):

    I enjoyed this paper and the approach to examining an accepted wisdom of ants determining overall density by employing age polyethism that would reduce the computational complexity required to match nest size with population (although I have some questions about the requirement that growth is infinite in such a solution). Moreover, the realization that models of collective behaviour may be inappropriate in many systems in which agents (or individuals) differ in the behavioural rules they employ, according to age, location, or information state. This is especially important in a system like social insects, typically held as a classic example of individual-as-subservient to whole, and therefore most likely to employ universal rules of behaviour. The current paper demonstrates a potentially continuous age-related change in target behaviour (excavation), and suggests an elegant and minimal solution to the requirement for building according to need in ants, avoiding the invocation of potentially complex cognitive mechanisms, or information states that all individuals must have access to in order to have an adaptive excavation output.

    The only real reservation I have is in the question of how this relationship could hold in properly mature colonies in which there is (presumably) a balance between the birth and death of older workers. Would the prediction be that the young ants still dig, or would there be a cessation of digging by young ants because the area is already sufficient? Another way of asking this is to ask whether the innate amount of digging that young ants do is in any way affected by the overall spatial size of the colony. If it is, then we are back to a problem of perfect information - how do the young ants know how big the overall colony is? Perhaps using density as a proxy? Alternatively, if the young ants do not modify their digging, wouldn't the colony become continuously larger? As a non-expert in social insects, I may be misunderstanding and it may be already addressed in the citations used.

    In any case, this is an excellent paper. The modelling approach is excellent and compelling, also allowing extrapolation to other group sizes and even other species. This to me is the main strength of the paper, as the answer to the question of whether it is younger or older ants that primarily excavate nests could have been answered by an individual tracking approach (albeit there are practical limitations to this, especially in the observation nest setup, as the authors point out). The analysis of the tunnel structure is also an important piece of the puzzle, and I really like the overall study.

  4. Reviewer #3 (Public review):

    Summary:

    In this study, Harikrishnan Rajendran, Roi Weinberger, Ehud Fonio, and Ofer Feinerman measured the digging behaviours of queens and workers for the first 6 months of colony development, as well as groups of young or old ants. They also provide a quantitative model describing the digging behaviours and allowing predictions. They found that young ants dig more slanted tunnels, while older ants dig more vertically (straight down). This finding is important, as it describes a new form of age polyethism (a division of labour based on age). Age polyethism is described as a "yes or no" mechanism, where individuals perform or not a task according to their age (usually young individuals perform in-nest tasks, and older ones foraging). Here, the way of performing the task is modified, not only the propensity to carry it or not. This data therefore adds in an interesting way to the field of collective behaviours and division of labour.

    The conclusions of the paper are well supported by the data. Measurements of the same individuals over time would have strengthened the claims.

    Strengths:

    I find that the measure of behaviour through development is of great value, as those studies are usually done at a specific time point with mature colonies. The description of a behaviour that is modified with age is a notable finding in the world of social insects. The sample sizes are adequate and all the information clearly provided either in the methods or supplementary.

    Weaknesses:

    I think the paper is failing to take into consideration or at least discuss the role of inter-individual variabilities. Tasks have been known to be undertaken by only a few hyper-active individuals for example. Comments on the choice to use averages and the potential roles of variations between individuals are in my opinion lacking. Throughout the paper wording should be modified to refer to the group and not the individuals, as it was the collective digging that was measured. Another issue I had was the use of "mature colony" for colonies with very few individuals and only 6 months of age. Comments on the low number of workers used compared to natural mature colonies would be welcome.

  5. Author response:

    Public Reviews:

    Reviewer #1 (Public review):

    This study investigates how ant group demographics influence nest structures and group behaviors of Camponotus fellah ants, a ground-dwelling carpenter ant species (found locally in Israel) that build subterranean nest structures. Using a quasi-2D cell filled with artificial sand, the authors perform two complementary sets of experiments to try to link group behavior and nest structure: first, the authors place a mated queen and several pupae into their cell and observe the structures that emerge both before and after the pupae eclose (i.e., "colony maturation" experiments); second, the authors create small groups (of 5,10, or 15 ants, each including a queen) within a narrow age range (i.e., "fixed demographic" experiments) to explore the dependence of age on construction. Some of the fixed demographic instantiations included a manually induced catastrophic collapse event; the authors then compared emergency repair behavior to natural nest creation. Finally, the authors introduce a modified logistic growth model to describe the time-dependent nest area. The modification introduces parameters that allow for age-dependent behavior, and the authors use their fixed demographic experiments to set these parameters, and then apply the model to interpret the behavior of the colony maturation experiments. The main results of this paper are that for natural nest construction, nest areas, and morphologies depend on the age demographics of ants in the experiments: younger ants create larger nests and angled tunnels, while older ants tend to dig less and build predominantly vertical tunnels; in contrast, emergency response seems to elicit digging in ants of all ages to repair the nest.

    We sincerely thank Reviewer #1 for the time and effort dedicated to our manuscript's detailed review and assessment. The revision suggestions were constructive, and we will incorporate them into the next version to improve the manuscript.

    Reviewer #2 (Public review):

    I enjoyed this paper and the approach to examining an accepted wisdom of ants determining overall density by employing age polyethism that would reduce the computational complexity required to match nest size with population (although I have some questions about the requirement that growth is infinite in such a solution). Moreover, the realization that models of collective behaviour may be inappropriate in many systems in which agents (or individuals) differ in the behavioural rules they employ, according to age, location, or information state. This is especially important in a system like social insects, typically held as a classic example of individual-as-subservient to whole, and therefore most likely to employ universal rules of behaviour. The current paper demonstrates a potentially continuous age-related change in target behaviour (excavation), and suggests an elegant and minimal solution to the requirement for building according to need in ants, avoiding the invocation of potentially complex cognitive mechanisms, or information states that all individuals must have access to in order to have an adaptive excavation output.

    We sincerely thank reviewer #2 for the time and effort dedicated to our manuscript's detailed review and assessment. The insightful feedback provided by the reviewer will be incorporated into the successive revisions.

    The only real reservation I have is in the question of how this relationship could hold in properly mature colonies in which there is (presumably) a balance between the birth and death of older workers. Would the prediction be that the young ants still dig, or would there be a cessation of digging by young ants because the area is already sufficient? Another way of asking this is to ask whether the innate amount of digging that young ants do is in any way affected by the overall spatial size of the colony. If it is, then we are back to a problem of perfect information - how do the young ants know how big the overall colony is? Perhaps using density as a proxy? Alternatively, if the young ants do not modify their digging, wouldn't the colony become continuously larger? As a non-expert in social insects, I may be misunderstanding and it may be already addressed in the citations used.

    We thank the reviewer for this interesting question. We find that the nest excavation is predominantly performed by the younger ants in the nest and the nest area increase is followed by an increase in the population. However, if the young ants dig unrestricted, this could result in unnecessary nest growth as suggested by reviewer #2. Therefore, we believe that the innate digging behavior of ants could potentially be regulated by various cues such as;

    (a) Density-based: If the colony becomes less dense as its area expands, this could serve as a feedback signal for young ants to reduce or stop digging, as described in references (25, 29, 30).

    (b) Pheromone depositions: If the colony reaches a certain population density, pheromone signals could inhibit further digging by young ants, references (25, 29,) or space usage as a proxy for the nest area.

    Thus, rather than perfect information, decentralized control, and digging-based local cues probably regulate the level of age-dependent digging, without the ants needing to estimate the overall colony size or nest area.

    In any case, this is an excellent paper. The modelling approach is excellent and compelling, also allowing extrapolation to other group sizes and even other species. This to me is the main strength of the paper, as the answer to the question of whether it is younger or older ants that primarily excavate nests could have been answered by an individual tracking approach (albeit there are practical limitations to this, especially in the observation nest setup, as the authors point out). The analysis of the tunnel structure is also an important piece of the puzzle, and I really like the overall study.

    We thank the reviewer for the comments. We completely agree that individual tracking of ants within our experimental setup would have been the ideal approach, but we were limited by technical and practical limitations of the setup as pointed out by the reviewer such as;

    (a) Continuous tracking of ants in our nests would have required a camera to be positioned at all times in front of the nest, which necessitates a light background. Since Camponotus fellah ants are subterranean, we aimed to allow them to perform nest excavation in conditions as close to their natural dark environment as possible. Additionally, implementing such a system in front of each nest would have reduced the sample sizes for our treatments.

    (b) The experimental duration of our colony maturation and fixed demographics experiments extended for up to six months (unprecedented durations in these kinds of measurements). These naturally limited our ability to conduct individual tracking while maintaining the identity of each ant based on the current design.

    Reviewer #3 (Public review):

    Summary:

    In this study, Harikrishnan Rajendran, Roi Weinberger, Ehud Fonio, and Ofer Feinerman measured the digging behaviours of queens and workers for the first 6 months of colony development, as well as groups of young or old ants. They also provide a quantitative model describing the digging behaviours and allowing predictions. They found that young ants dig more slanted tunnels, while older ants dig more vertically (straight down). This finding is important, as it describes a new form of age polyethism (a division of labour based on age). Age polyethism is described as a "yes or no" mechanism, where individuals perform or not a task according to their age (usually young individuals perform in-nest tasks, and older ones foraging). Here, the way of performing the task is modified, not only the propensity to carry it or not. This data therefore adds in an interesting way to the field of collective behaviours and division of labour.

    The conclusions of the paper are well supported by the data. Measurements of the same individuals over time would have strengthened the claims.

    We sincerely thank reviewer #3 for the time and effort dedicated to our manuscript's detailed review and assessment. We completely agree with the reviewer’s comments on the measurements of the same individuals over time, however, we were limited by the technical and experimental limitations as described above and pointed out by reviewer #2.

    Strengths:

    I find that the measure of behaviour through development is of great value, as those studies are usually done at a specific time point with mature colonies. The description of a behaviour that is modified with age is a notable finding in the world of social insects. The sample sizes are adequate and all the information clearly provided either in the methods or supplementary.

    We thank the reviewer #3 for this assessment.

    Weaknesses:

    I think the paper is failing to take into consideration or at least discuss the role of inter-individual variabilities. Tasks have been known to be undertaken by only a few hyper-active individuals for example. Comments on the choice to use averages and the potential roles of variations between individuals are in my opinion lacking. Throughout the paper wording should be modified to refer to the group and not the individuals, as it was the collective digging that was measured. Another issue I had was the use of "mature colony" for colonies with very few individuals and only 6 months of age. Comments on the low number of workers used compared to natural mature colonies would be welcome.

    Regarding main comment 1

    We completely agree with the reviewer’s comment on considering inter-individual variability based on activity levels. We have discussed how individual morphological variability could influence digging behavior (references: 28, 31), and we will elaborate further on this aspect in future revisions.

    Regarding main comment 2:

    We agree with the reviewer’s comments regarding the wording. The term “mature colony” will be revised in future versions. The wording (“mature colony”‘) will be changed and addressed in the future revisions. We were practically limited by the continuation of the experiments for more than 6 months of age predominantly due to the stability of nests as they were made with a sand-soil mix. We also acknowledge that the colony sizes attained in our maturation experiments may be smaller than those of naturally matured colonies. This trend was observed generally in lab-reared colonies and could be attributed to differences in microclimatic conditions, foraging opportunities, space availability, and other factors. We will address these aspects in more detail in future revisions.