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  1. Alarm signal propagation through ant colonies provides an empirically tractable context for analysing information flow through a natural system, with useful insights for network dynamics in other social animals. Here, we develop a methodological approach to track alarm spread within a group of harvester ants, Pogonomyrmex californicus . We initially alarmed three ants and tracked subsequent signal transmission through the colony. Because there was no actual standing threat, the false alarm allowed us to assess amplification and adaptive damping of the collective alarm response. We trained a random forest regression model to quantify alarm behaviour of individual workers from multiple movement features. Our approach translates subjective categorical alarm scores into a reliable, continuous variable. We combined these assessments with automatically tracked proximity data to construct an alarm propagation network. This method enables analyses of spatio-temporal patterns in alarm signal propagation in a group of ants and provides an opportunity to integrate individual and collective alarm response. Using this system, alarm propagation can be manipulated and assessed to ask and answer a wide range of questions related to information and misinformation flow in social networks. 
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  2. Fear of predation may assert privilege to prey species by restricting their exposure to potential predators, meanwhile it can also impose costs by constraining the exploration of optimal resources. A predator–prey model with the effect of fear, refuge, and hunting cooperation has been investigated in this paper. The system’s equilibria are obtained and their local stability behavior is discussed. The existence of Hopf-bifurcation is analytically shown by taking refuge as a bifurcation parameter. There are many ecological factors which are not instantaneous processes, and so, to make the system more realistic, we incorporate three discrete time delays: in the effect of fear, refuge and hunting cooperation, and analyze the delayed system for stability and bifurcation. Moreover, for environmental fluctuations, we further modify the delayed system by incorporating seasonality in the fear, refuge and cooperation. We have analyzed the seasonally forced delayed system for the existence of a positive periodic solution. In the support of analytical results, some numerical simulations are carried out. Sensitivity analysis is used to identify parameters having crucial impacts on the ecological balance of predator–prey interactions. We find that the rate of predation, fear, and hunting cooperation destabilizes the system, whereas prey refuge stabilizes the system. Time delay in the cooperation behavior generates irregular oscillations whereas delay in refuge stabilizes an otherwise unstable system. Seasonal variations in the level of fear and refuge generate higher periodic solutions and bursting patterns, respectively, which can be replaced by simple 1-periodic solution if the cooperation and fear are also allowed to vary with time in the former and latter situations. Higher periodicity and bursting patterns are also observed due to synergistic effects of delay and seasonality. Our results indicate that the combined effects of fear, refuge and hunting cooperation play a major role in maintaining a healthy ecological environment. 
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  3. Western honeybees (Apis Mellifera) serve extremely important roles in our ecosystem and economics as  they are responsible for pollinating $ 215 billion dollars annually over the world.  Unfortunately,  honeybee population and their colonies have been declined dramatically. The purpose of this article is to explore how we should model honeybee population with age structure and validate the model using empirical data so that we can identify different factors that lead to the survival and healthy of the honeybee colony.  Our theoretical study combined with simulations and data validation suggests that the proper age structure incorporated in the model  and seasonality are important for modeling honeybee population.  Specifically, our work implies that the model assuming that (1) the adult bees are survived from the egg population rather than the brood population; and (2) seasonality in the queen egg laying rate, give the better fit than other honeybee models. The related theoretical and numerical analysis of the most fit model indicate that (a) the survival of honeybee colonies requires a large queen egg-laying rate and smaller values of the other life history parameter values in addition to proper initial condition; (b) both brood and adult bee populations are increasing with respect to the increase in the egg-laying rate and the decreasing in other parameter values; and (c) seasonality may promote/suppress the survival of the honeybee colony. 
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