Abstract

I focus on the foraging efficiency (food intake per time) of a hypothetical forager that uses distinct levels of information about a set of discrete renewing resources. The information may be the distance to the resource (D), both distance and maximum productivity of the resource (DP), or distance, productivity, and the elapsed time since the forager last visited each resource (DPT). The expected foraging efficiencies are based on the results of a field experiment on wild capuchin monkeys (Janson 2016) that documented the use of integrative memories of resource location, productivity, and elapsed time since the previous visit. Computer simulations of the choice process are used to extend the resource parameter space beyond the field experiment. The goal is to explore to what extent the use of elapsed time in choosing discrete feeding sites is a benefit under various conditions of resource and consumer characteristics. Major findings include that the use of elapsed time generally increases foraging efficiency on renewing resources by 30-35%, without much effect of resource size or variability – indeed, DPT outperforms D or DP choice even when all resources have the same productivity. The relative benefit of DPT increases when the most productive resources are only moderately common (not so rare that they contribute little to food intake, nor so common that choosing the nearest resource is likely to arrive at a highly productive one). The relative benefit of DPT decreases when the forager’s gut capacity is small or gut passage time is long because it cannot fully ingest large resource accumulations that occur after long elapsed intervals. I suggest that memory for and use of elapsed intervals since prior visits in foraging choices will prove to be a common feature of diverse foraging animals whenever the presence of a forager depresses food availability in a local area.

Highlights

  • One of the persistent mysteries about primates is why, as an order, they have evolved relatively large brains for their body size compared to most other mammals (e.g., Martin, 1981; Allman, 1999)

  • I use three multinomial logistic regressions using observed movement choices between provisioned feeding sites to fit the effects on site choice of (1) food site distance alone (D), (2) distance plus provisioning treatment (DP), and (3) distance, provisioning treatment, and elapsed time (DPT)

  • To convert expected reward and distance to more conventional measures of foraging efficiency, I use the facts that feeding time increases predictably with the amount eaten at each site (Methods), and that travel speed between sites does not depend predictably on the particular pair of sites chosen but only on the distance between them (Janson, 2016a)

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Summary

INTRODUCTION

One of the persistent mysteries about primates is why, as an order, they have evolved relatively large brains for their body size compared to most other mammals (e.g., Martin, 1981; Allman, 1999). Some primates apparently keep track of seasonal patterns of fruiting of at least a few of their food species (e.g., Menzel, 1991; Janmaat et al, 2011), and may even anticipate different rates of ripening according to weather conditions (Janmaat et al, 2006b) Both of these kinds of knowledge require updating the productivity status of resources, implying dynamic “where-what” memory, but they do not necessarily require keeping track of elapsed time since a previous feeding visit, which might imply “where-what-when” memory. I use computer simulations to mimic the foraging decisions of a hypothetical primate in a field of renewing food patches if it were to use only “where,” “where-what,” or “where-what-when” memory This approach allows me to verify the results I found in the field experiment (Janson, 2016a) and to expand the range of possible resource parameters to test how the relative foraging efficiencies of distinct cognitive foraging decisions depend on ecological context

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