scholarly journals Regulation of Harvester Ant Foraging as a Closed-Loop Excitable System

2018 ◽  
Author(s):  
Renato Pagliara ◽  
Deborah M. Gordon ◽  
Naomi Ehrich Leonard

AbstractAnt colonies regulate activity in response to changing conditions without using centralized control. Harvester ant colonies forage in the desert for seeds, and their regulation of foraging manages a tradeoff between spending and obtaining water. Foragers lose water while outside in the dry air, but the colony obtains water by metabolizing the fats in the seeds they eat. Previous work shows that the rate at which an outgoing forager leaves the nest depends on its recent experience of brief antennal contact with returning foragers that carry a seed. We examine how this process can yield foraging rates that are robust to uncertainty and responsive to temperature and humidity across minutes to hour-long timescales. To explore possible mechanisms, we develop a low-dimensional analytical model with a small number of parameters that captures observed foraging behavior. The model uses excitability dynamics to represent response to interactions inside the nest and a random delay distribution to represent foraging time outside the nest. We show how feedback of outgoing foragers returning to the nest stabilizes the incoming and outgoing foraging rates to a common value determined by the “volatility” of available foragers. The model exhibits a critical volatility above which there is sustained foraging at a constant rate and below which there is cessation of foraging. To explain how the foraging rates of colonies adjust to temperature and humidity, we propose a mechanism that relies on foragers modifying their volatility after they leave the nest and get exposed to the environment. Our study highlights the importance of feedback in the regulation of foraging activity and points to modulation of volatility as a key to explaining differences in foraging activity in response to conditions and across colonies. Our results present opportunities for generalization to other contexts and systems with excitability and feedback across multiple timescales.Author SummaryWe investigate the collective behavior that allows colonies of desert harvester ants to regulate foraging activity in response to environmental conditions. We develop an analytical model connecting three processes: 1) the interactions between foragers returning to the nest and available foragers waiting inside the nest, 2) the effect of these interactions on the likelihood of available foragers to leave the nest to forage, and 3) the return of foragers to the nest after finding seeds. We propose a mechanism in which available foragers modify their response to interactions after their first exposure to the environment. We show how this leads to colony foraging rates that adjust to environmental conditions over time scales from minutes to hours. Our model may prove useful for studying resilience in other classes of systems with excitatory dynamics.

2015 ◽  
Vol 11 (10) ◽  
pp. 20150695 ◽  
Author(s):  
Noa Pinter-Wollman

Structures influence how individuals interact and, therefore, shape the collective behaviours that emerge from these interactions. Here I show that the structure of a nest influences the collective behaviour of harvester ant colonies. Using network analysis, I quantify nest architecture and find that as chamber connectivity and redundancy of connections among chambers increase, so does a colony's speed of recruitment to food. Interestingly, the volume of the chambers did not influence speed of recruitment, suggesting that the spatial organization of a nest has a greater impact on collective behaviour than the number of workers it can hold. Thus, by changing spatial constraints on social interactions organisms can modify their behaviour and impact their fitness.


1995 ◽  
Vol 198 (2) ◽  
pp. 521-530 ◽  
Author(s):  
J Lighton ◽  
D Berrigan

Do developmental constraints in ant colonies limit gas exchange strategies to those displayed by female alates (presumptive queens)? In the xeric harvester ant genus Messor, we found that M. pergandei and M. julianus female alates ventilated highly discontinuously, as predicted, but M. julianus workers ventilated less discontinuously and M. pergandei workers (which occur in more xeric habitats) ventilated continuously. We present the salient characteristics of the discontinuous ventilation cycles of the species and the manner in which they are modulated by CO2 emission rates at a single temperature (24 °C). We demonstrate that, in M. julianus workers, open-spiracle phase CO2 emission rate only slightly exceeds overall CO2 emission rate, making discontinuous ventilation marginal, a state extrapolated in M. pergandei to continuous ventilation. However, workers are plainly capable of far greater rates of CO2 emission than when inactive at 24 °C, so the lack of discontinuous ventilation in M. pergandei under normoxic conditions is not likely to be imposed by physiological constraints and may, in fact, be a response to its xeric environment. We hypothesize ­ aside from phylogenetic effects ­ that discontinuous ventilation occurs primarily in insects that may experience hypoxic and hypercapnic conditions, such as ant queens during claustral colony foundation and perhaps workers within the nest environment; that discontinuous ventilation is not necessarily essential to reduce respiratory water loss; and that it will not necessarily occur in castes or species routinely exposed to xeric but normoxic conditions.


Energies ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 2071
Author(s):  
Brian Fiedler

The simplest model for an atmospheric boundary layer assumes a uniform steady wind over a certain depth, of order 1 km, with the forces of friction, pressure gradient and Coriolis in balance. A linear model is here employed for the adjustment of wind to this equilibrium, as the wake of a very wide wind farm. A length scale is predicted for the exponential adjustment to equilibrium. Calculation of this length scale is aided by knowledge of the angle for which the wind would normally cross the isobars in environmental conditions in the wake.


2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Javed Riaz ◽  
Sophie Bestley ◽  
Simon Wotherspoon ◽  
Louise Emmerson

Abstract Background Diving marine predators forage in a three-dimensional environment, adjusting their horizontal and vertical movement behaviour in response to environmental conditions and the spatial distribution of prey. Expectations regarding horizontal-vertical movements are derived from optimal foraging theories, however, inconsistent empirical findings across a range of taxa suggests these behavioural assumptions are not universally applicable. Methods Here, we examined how changes in horizontal movement trajectories corresponded with diving behaviour and marine environmental conditions for a ubiquitous Southern Ocean predator, the Adélie penguin. Integrating extensive telemetry-based movement and environmental datasets for chick-rearing Adélie penguins at Béchervaise Island, we tested the relationships between horizontal move persistence (continuous scale indicating low [‘resident’] to high [‘directed’] movement autocorrelation), vertical dive effort and environmental variables. Results Penguins dived continuously over the course of their foraging trips and lower horizontal move persistence corresponded with less intense foraging activity, likely indicative of resting behaviour. This challenges the traditional interpretation of horizontal-vertical movement relationships based on optimal foraging models, which assumes increased residency within an area translates to increased foraging activity. Movement was also influenced by different environmental conditions during the two stages of chick-rearing: guard and crèche. These differences highlight the strong seasonality of foraging habitat for chick-rearing Adélie penguins at Béchervaise Island. Conclusions Our findings advance our understanding of the foraging behaviour for this marine predator and demonstrates the importance of integrating spatial location and behavioural data before inferring habitat use.


2004 ◽  
Vol 36 (5) ◽  
pp. 797-804 ◽  
Author(s):  
Diane Wagner ◽  
Jeremy B Jones ◽  
Deborah M Gordon

2012 ◽  
Vol 23 (5) ◽  
pp. 1022-1029 ◽  
Author(s):  
Noa Pinter-Wollman ◽  
Deborah M. Gordon ◽  
Susan Holmes
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